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O - Environmental Thesaurus (ENVTHES)
http://vocabs.lter-europe.net/EnvThes/EUUnits_198
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O horizon - ENVTHES
http://vocabs.lter-europe.net/EnvThes/40
[Agren & Andersson 2012] Accumulation of litter and particular decomposed plant parts on top of the mineral soil. Often sub-divided into litter (S, L and F) and humus (H) horizons. This horizon consists mostly of organic matter. In forest soils, this horizon is often called forest floor
Phosphorodithioic acid O,O-diesters - Chemical Functional Ontology (CHEMFONT)
http://purl.obolibrary.org/obo/CHEMONTID_0004662
Organooxygen compounds that contain a phosphorodithioic acid, which is O,O-disubstituted by an organyl group.
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O-phenylenediamines - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004746
Aromatic compound containing a benzene ring which carries 2 amino groups, at the 1- and 2-positions.
o-Xylenes - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004210
Aromatic compounds that contain a o-xylene moiety, which is a monocyclic benzene carrying exactly two methyl groups at the 1- and 2-positions.
O-quinodimethanes - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0001778
Compounds containing a benzene ring conjugated to two methylidene groups at carbon atoms 1 and 2, respectively.
O-thiocarbamates - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004425
O-ester derivatives of thiocarbamic acid, with the general formula ROC(=S)NR2.
O-terphenyls - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0001836
Terphenyls with a structure containing the 1,2-diphenylbenzene skeleton.
O-glucuronides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002813
Glucuronides in which the aglycone is linked to the carbohydrate unit through an O-glycosidic bond.
o-Toluamides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004221
Aromatic compounds containing a toluene, which carries a carboxamide group a the 2-position.
o-Aminophenols - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004654
Phenols that are substituted with an amine group at the 2-position of the benzene ring.
O-iodophenols - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002777
Iodophenols carrying a iodine at the C2 position of the benzene ring.
O-haloacetanilides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004718
Organic compounds containing an acetamide group conjugated to a phenyl group, which is in turn ortho-substituted with a halogen atom.
O-quinomethanes - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002122
Organic compounds containing a benzene ring conjugated to a methylidene group and a ketone at carbon atoms 1 and 2, respectively.
O-iminoquinones - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002388
O-quinones that carry an imine group.
O-bromophenols - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002768
Bromophenols carrying a iodine at the C2 position of the benzene ring.
O-quinonimines - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002894
Quinonimines in which the imine groups are in a ortho-relationship.
O-phenylhydroxylamines - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004651
Hydroxylamines that are O-substituted with a phenyl group.
O-alkylglycerones - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003445
Organic compounds containing a glycerone that carries an acyl substituent at the 1-position or the 2-position.
o-Xylenols - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004214
Aromatic compounds that contain a o-xylenol moiety, which is a monocyclic benzene carrying exactly two methyl groups at the 1- and 2-positions, and at least one hydroxyl group.
O-quinones - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002385
Quinones where the two C=O groups are attached at the 1- and 2-positions, respectively.
O-chlorophenols - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002771
Chlorophenols carrying a iodine at the C2 position of the benzene ring.
O-benzoquinones - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002492
Benzoquinones where the two C=O groups are attached at the 1- and 2-positions, respectively.
O-fluorophenols - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002774
Fluorophenols carrying a iodine at the C2 position of the benzene ring.
O-alkylpyrimidines - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004486
Compounds containing a pyrimidine , which is O-alkylated at one or more ring positions.
Rotenoid O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0001741
Compounds containing a carbohydrate moiety glycosidically linked to the rotenoid backbone at the C8-position.
O-alkylglycerone phosphates - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003447
Glycerone-3-phosphates carrying an alkyl substituent at the 1-position.
7-O-methylisoflavones - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002689
Isoflavones with methoxy groups attached to the C7 atom of the isoflavone backbone.
Sulfonohydrazonothioic o-acids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003144
Organic acids with the general formula RS(S)(=NH2)-OH (R=H, organic group).
Thiosulfonimidic o-acids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002531
Organic compounds with the general formula HOS(R)(=N)(=S) (R = alkyl, aryl).
Sulfonothioic O-acids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004357
Organosulfur compounds with the general formula RS(O)(S)-OH.
O-acylglycerone-phosphates - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003448
Glycerone-3-phosphates carrying an acyl substituent at the 1-position.
O-coumaroyl glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002684
Glycosides of o-coumaric acids. O-coumaric acids are aromatic compounds containing a cinnamic acid moiety hydroxylated at the C2 carbon atom of the benzene ring.
Iridoid O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004081
Iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton.
Carbothioic O-acids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003108
Organic acids with the general formula RCO-SH (R=H, organic group).
Dithiophosphate O-esters - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004164
O-ester derivatives of dithiophosphates, with the general structure RSP(O)(O)=S (R = organyl group).
3'-O-methylisoflavones - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002690
Flavones with methoxy groups attached to the C2' atom of the isoflavone backbone.
Aurone O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0001738
Aurone flavonoids containing a carbohydrate moiety O-glycosidically bound to the aurone skeleton.
Dithiosulfonic O-acids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002543
Organic acids with the general formula RS(=S)(=S)OH.
Flavonoid O-glucuronides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002934
Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid.
Flavonoid O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0001583
Compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.
O-methylated flavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002585
Flavonoids with methoxy groups conjugated to the flavonoid backbone.
O-methylated isoflavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002586
Isoflavonoids with methoxy groups conjugated to the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
O-cinnamoyl glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003479
O-glycoside derivatives of cinnamic acid. Cinnamic acid is an aromatic compound containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid.
Carbothioic O-lactones - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003875
Cyclic organosulfur compounds with the general structure RC(=S)OR', R-R' = organyl group, where the central atom is part of the ring.
sterol O-acyltransferase - CHEMFONT
file:/home/william/Workspace/chemont/HGNC.owl#HGNC_sterol_O-acyltransferase_
o-Phthalate esters - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004011
Ester derivatives of o-phthalic acids, which are based on a benzene 1,2-dicarboxylic acid skeleton.
4'-O-methylisoflavones - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002687
Isoflavones with methoxy groups attached to the C4' atom of the isoflavone backbone.
1-O-alkylglycerols - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004274
Glycerolipids containing a glycerol moiety that carries an alkyl group at the 1-position.
Carbothioic O-esters - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003874
Ester derivatives of carbothioic O-acids, with the general structure ROC(=S)R' where R = organyl group and R' = H or organyl group.
Benzo-o-dioxins - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0001382
Organic compounds containing a benzene ring fused to a 1,2-dioxin ring.
O-sulfanylbenzoic acids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003106
Benzoic acids which bear a sulfanyl group (R-SH) attached to the benzene ring at positions 1 and 2, respectively.
Isoflavonoid O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0000507
O-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.
O-glycosyl compounds - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002207
Glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.
4-O-methylated flavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002589
Flavonoids with methoxy groups attached to the C4 atom of the flavonoid backbone.
Flavonoid-7-O-glucuronides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003534
Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid at the C7-position.
5-O-methylated isoflavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002600
Isoflavonoids with methoxy groups attached to the C5 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
o-Hydroxybenzoic acid esters - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004700
Benzoic acid esters where the benzene ring is ortho-substituted with a hydroxy group.
4'-O-methylated isoflavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002606
Isoflavonoids with methoxy groups attached to the C4' atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
3'-O-methylated flavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002595
Flavonoids with methoxy groups attached to the C3' atom of the flavonoid backbone.
6-O-methylated isoflavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002601
Isoflavonoids with methoxy groups attached to the C6 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
5-O-methylated flavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002590
Flavonoids with methoxy groups attached to the C5 atom of the flavonoid backbone.
Phosphoramidothioic acid O-esters - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004664
Organooxygen compounds containing a O-ester derivative of phosphoroamidothioic acid. They have the general structure ROP(=O)(S)(NH2), where R is an organyl group.
Neoflavonoid 5-O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002897
5-O-glycosylated neoflavonoids. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.
Flavonoid-8-O-glucuronides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003541
Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid at the C8-position.
4'-O-methylated flavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002596
Flavonoids with methoxy groups attached to the C4' atom of the flavonoid backbone.
Membrane bound O-acyltransferases - CHEMFONT
file:/home/william/Workspace/chemont/HGNC.owl#HGNC_1036
Flavonoid-3-O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003531
Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position.
Benzofuran-5-O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003500
Benzofurans that a O-glycosylated at the 2-position. Benzofurans are organic compounds containing a benzene ring fused to a furan.
Hydroxylamine O-sulfonic acids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003110
Sulfonic acids with the general formula R-N-OS(O)(=O)=O. They can be synthesized through reaction of hydroxylamine and chlorosulfonic acids.
Anthocyanidin-5-O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002997
Phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C5-position.
Flavonoid-3-O-glucuronides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003532
Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid at the C3-position.
Anthocyanin-4'-O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003552
Phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C4'-position.
2-O-methylated flavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002587
Flavonoids with methoxy groups attached to the C2 atom of the flavonoid backbone.
7-O-methylated isoflavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002602
Isoflavonoids with methoxy groups attached to the C7 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
6-O-methylated flavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002591
Flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone.
8-O-methylated isoflavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002603
Isoflavonoids with methoxy groups attached to the C8 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
7-O-methylated flavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002592
Flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone.
Flavonoid-7-O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003533
Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position.
3-O-methylated isoflavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002598
Isoflavonoids with methoxy groups attached to the C3 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
8-O-methylated flavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002593
Flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone.
4-O-methylated isoflavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002599
Isoflavonoids with methoxy groups attached to the C4 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
3'-O-methylated isoflavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002605
Isoflavonoids with methoxy groups attached to the C3' atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
2'-O-methylated flavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002594
Flavonoids with methoxy groups attached to the C2' atom of the flavonoid backbone.
Organic O-nitroso compounds - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004778
Organic compounds containing a n-nitroso group -ON=O.
Flavonoid-8-O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003540
Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C8-position.
Anthocyanidin-3-O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002996
Phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C3-position.
Anthocyanin-3'-O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003551
Phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C3'-position.
Neoflavonoid 7-O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002935
7-O-glycosylated neoflavonoids. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.
2'-O-methylated isoflavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002604
Isoflavonoids with methoxy groups attached to the C2' atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
Phosphorodithioic acid O-monoesters - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004661
Organooxygen compounds that contain a phosphorodithioic acid, which is O-monosubstituted by an organyl group.
2-O-methylated isoflavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002597
Isoflavonoids with methoxy groups attached to the C2 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
Anthocyanidin-7-O-Glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003555
Phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C7-position.
Benzofuran-2-O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003498
Benzofurans that a O-glycosylated at the 2-position. Benzofurans are organic compounds containing a benzene ring fused to a furan.
N-alkyl-O-phenylhydroxylamines - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004652
Hydroxylamines that are O-substituted with a phenyl group, and N-substituted by an alkyl group.
3-O-methylated flavonoids - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002588
Flavonoids with methoxy groups attached to the C3 atom of the flavonoid backbone.
O-phthalic acid and derivatives - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0001107
Compounds containing a benzene ring bearing a carboxylic acid group at ring carbon atoms 1 and 3.
Phosphoramidothioic-acid-O,S-diesters - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004665
Organooxygen compounds containing a O,S-diester derivative of phosphoroamidothioic acid. They have the general structure RSP(=O)(OR')(NH2), where R,R' are organyl groups.
O-methoxybenzoic acids and derivatives - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002345
Benzoic acids in which the hydrogen atom at position 2 of the benzene ring is replaced by a methoxy group.
1-O-alkyl-sn-glycerols - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004275
Glycerolipids containing a chiral glycerol moiety that carries an alkyl group at the 1-position.
O-galloylquinic acids and derivatives - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002513
Compounds containing a galloic acid moiety, linked to one hydroxyl group of a quinic acid moiety.
Chalcone- and dihydrochalcone O-glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0001739
Compounds containing a O-glycosylated chalcone or dihydrochalcone moiety.
O-sulfanylbenzoic acids and derivatives - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003105
Benzoic acids (or derivatives) which bear a sulfanyl group (R-SH) attached to the benzene ring at positions 1 and 2, respectively.
5'-O-tritylated nucleosides and derivatives - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0004232
Ribonucleosides or derivatives, in which the ribose moiety carries a trityl group at the 5' position, and is N-linked at the to either a purine or a pyrimidine base.
Anthocyanidin 7-O-p-coumaroyl glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003556
Anthocyanidin 7-O-glycosides where the carbohydrate moiety is esterified with a p-coumaric acid. P-coumaric acid is an organic derivative of cinnamic acid, that carries a hydroxyl group at the 4-position of the benzene ring.
Flavonoid 3p-O-p-coumaroyl glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0003681
Flavonoid 3p-O-glycosides where the carbohydrate moiety is esterified with a p-coumaric acid. P-coumaric acid is an organic derivative of cinnamic acid, that carries a hydroxyl group at the 4-position of the benzene ring.
Anthocyanidin 3-O-p-coumaroyl glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002708
Anthocyanidin 3-O-glycosides where the carbohydrate moiety is esterified with a p-coumaric acid. P-coumaric acid is an organic derivative of cinnamic acid, that carries a hydroxyl group at the 4-position of the benzene ring.
Anthocyanidin 3p-O-p-coumaroyl glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002709
Anthocyanidin 3p-O-glycosides where the carbohydrate moiety is esterified with a p-coumaric acid. P-coumaric acid is an organic derivative of cinnamic acid, that carries a hydroxyl group at the 4-position of the benzene ring.
Anthocyanidin 5-O-p-coumaroyl glycosides - CHEMFONT
http://purl.obolibrary.org/obo/CHEMONTID_0002710
Anthocyanidin 5-O-glycosides where the carbohydrate moiety is esterified with a p-coumaric acid. P-coumaric acid is an organic derivative of cinnamic acid, that carries a hydroxyl group at the 4-position of the benzene ring.
o-tolualdehyde - ACTRIS Vocabulary (ACTRIS_VOCAB)
https://vocabulary.actris.nilu.no/actris_vocab/o-tolualdehyde
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o-cresol - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-cresol
o-xylene - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-xylene
o,p-DDT - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-p-DDT
o,p-DDD - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-p-DDD
tetrabromo-o-chlorotoluene - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/tetrabromo-o-chlorotoluene
o,p-DDE - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-p-DDE
o-tolualdehyde amount fraction - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-tolualdehydeamountfraction
Amount fraction is used in the construction mole_fraction_of_X_in_Y, where X is a material constituent of Y. The chemical formula for o-tolualdehyde is C8H8O. O-tolualdehyde is a member of the group of aldehydes. The IUPAC name for o-tolualdehyde is 2-methylbenzaldehyde.
o-xylene amount fraction - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-xyleneamountfraction
Amount fraction is used in the construction mole_fraction_of_X_in_Y, where X is a material constituent of Y. The chemical formula for o-xylene is C8H10. O-xylene is a member of the group of hydrocarbons known as aromatics. The IUPAC name for 1,2-xylene.
o-tolualdehyde number concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-tolualdehydenumberconcentration
Number concentration means number of molecule per unit volume, and is used in the construction molecular_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chemical formula for o-tolualdehyde is C8H8O. O-tolualdehyde is a member of the group of aldehydes. The IUPAC name for o-tolualdehyde is 2-methylbenzaldehyde.
o-cresol mass concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-cresolmassconcentration
Mass concentration means mass per unit volume and is used in the construction mass_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chemical formula for o-cresol is C7H8O. O-cresol is a member of the group of alcohols. The IUPAC name for o-cresol is 2-methylphenol.
o-cresol number concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-cresolnumberconcentration
Number concentration means number of molecule per unit volume, and is used in the construction molecular_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chemical formula for o-cresol is C7H8O. O-cresol is a member of the group of alcohols. The IUPAC name for o-cresol is 2-methylphenol.
o-xylene mass concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-xylenemassconcentration
Mass concentration means mass per unit volume and is used in the construction mass_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chemical formula for o-xylene is C8H10. O-xylene is a member of the group of hydrocarbons known as aromatics. The IUPAC name for o-xylene is 1,2-xylene.
o-xylene number concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-xylenenumberconcentration
Number concentration means number of molecule per unit volume, and is used in the construction molecular_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chemical formula for o-xylene is C8H10. O-xylene is a member of the group of hydrocarbons known as aromatics. The IUPAC name for o-xylene is 1,2-xylene.
o-tolualdehyde mass concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-tolualdehydemassconcentration
Mass concentration means mass per unit volume and is used in the construction mass_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chemical formula for o-tolualdehyde is C8H8O. O-tolualdehyde is a member of the group of aldehydes. The IUPAC name for o-tolualdehyde is 2-methylbenzaldehyde.
o-cresol amount fraction - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-cresolamountfraction
Amount fraction is used in the construction mole_fraction_of_X_in_Y, where X is a material constituent of Y. The chemical formula for o-cresol is C7H8O. O-cresol is a member of the group of alcohols. The IUPAC name for o-cresol is 2-methylphenol.
gaseous o,p-DDD mass concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-p-DDDmassconcentration
Mass concentration means mass per unit volume and is used in the construction mass_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chmical formula for o,p-DDD is C14H10Cl4. It is a member of the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2-dichloro-1-(4-chlorophenyl)ethyl]benzene
precipitation o,p-DDD mass concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/precipitationo-p-DDDmassconcentration
Mass concentration means mass per unit volume and is used in the construction mass_ concentration_ of_ X_ in_ Y, where X is a material constituent of Y. Precipitation is liquid or frozen water that forms in the atmosphere and falls to the earth. It comes in many forms, like rain, snow, and sleet. The chmical formula for o,p-DDD is C14H10Cl4. It belongs to the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2-dichloro-1-(4-chlorophenyl)ethyl]benzene
gaseous o,p-DDE amount fraction - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-p-DDEamountfraction
Amount fraction is used in the construction mole_fraction_of_X_in_Y, where X is a material constituent of Y. The chmical formula for o,p-DDE is C14H8Cl4. It is a member of the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2-dichloro-1-(4-chlorophenyl)ethenyl]benzene
moss o,p-DDT mass fraction - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/mosso-p-DDTmassfraction
Moss X mass fraction is the ratio of mass of a substance X to the total mass of the dried moss. The chmical formula for o,p-DDT is C14H9Cl5. It belongs to the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2,2-trichloro-1-(4-chlorophenyl)ethyl]benzene
moss o,p-DDE mass fraction - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/mosso-p-DDEmassfraction
Moss X mass fraction is the ratio of mass of a substance X to the total mass of the dried moss. The chmical formula for o,p-DDE is C14H8Cl4. It belongs to the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2-dichloro-1-(4-chlorophenyl)ethenyl]benzene
gaseous tetrabromo-o-chlorotoluene mass concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/tetrabromo-o-chlorotoluenemassconcentration
Mass concentration means mass per unit volume and is used in the construction mass_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chmical formula for tetrabromo-o-chlorotoluene is C7H3Br4Cl. It is a member of the group of halogenated organics and aromatics. The IUPAC name is 1,2,3,4-tetrabromo-5-chloro-6-methylbenzene
gaseous o,p-DDD amount fraction - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-p-DDDamountfraction
Amount fraction is used in the construction mole_fraction_of_X_in_Y, where X is a material constituent of Y. The chmical formula for o,p-DDD is C14H10Cl4. It is a member of the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2-dichloro-1-(4-chlorophenyl)ethyl]benzene
gaseous tetrabromo-o-chlorotoluene amount fraction - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/tetrabromo-o-chlorotolueneamountfraction
Amount fraction is used in the construction mole_fraction_of_X_in_Y, where X is a material constituent of Y. The chmical formula for tetrabromo-o-chlorotoluene is C7H3Br4Cl. It is a member of the group of halogenated organics and aromatics. The IUPAC name is 1,2,3,4-tetrabromo-5-chloro-6-methylbenzene
gaseous o,p-DDD number concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-p-DDDnumberconcentration
Number concentration means number of molecule per unit volume, and is used in the construction molecular_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chmical formula for o,p-DDD is C14H10Cl4. It is a member of the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2-dichloro-1-(4-chlorophenyl)ethyl]benzene
moss o,p-DDD mass fraction - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/mosso-p-DDDmassfraction
Moss X mass fraction is the ratio of mass of a substance X to the total mass of the dried moss. The chmical formula for o,p-DDD is C14H10Cl4. It belongs to the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2-dichloro-1-(4-chlorophenyl)ethyl]benzene
gaseous o,p-DDT number concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-p-DDTnumberconcentration
Number concentration means number of molecule per unit volume, and is used in the construction molecular_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chmical formula for o,p-DDT is C14H9Cl5. It is a member of the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2,2-trichloro-1-(4-chlorophenyl)ethyl]benzene
precipitation o,p-DDE mass concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/precipitationo-p-DDEmassconcentration
Mass concentration means mass per unit volume and is used in the construction mass_ concentration_ of_ X_ in_ Y, where X is a material constituent of Y. Precipitation is liquid or frozen water that forms in the atmosphere and falls to the earth. It comes in many forms, like rain, snow, and sleet. The chmical formula for o,p-DDE is C14H8Cl4. It belongs to the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2-dichloro-1-(4-chlorophenyl)ethenyl]benzene
pentanal and o-tolualdehyde number concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/pentanalando-tolualdehydenumberconcentration
Number concentration means number of molecule per unit volume, and is used in the construction molecular_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. Pentanal and o-tolualdehyde is a mixture of two compunds in the group of aldehydes.
gaseous tetrabromo-o-chlorotoluene number concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/tetrabromo-o-chlorotoluenenumberconcentration
Number concentration means number of molecule per unit volume, and is used in the construction molecular_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chmical formula for tetrabromo-o-chlorotoluene is C7H3Br4Cl. It is a member of the group of halogenated organics and aromatics. The IUPAC name is 1,2,3,4-tetrabromo-5-chloro-6-methylbenzene
gaseous o,p-DDE mass concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-p-DDEmassconcentration
Mass concentration means mass per unit volume and is used in the construction mass_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chmical formula for o,p-DDE is C14H8Cl4. It is a member of the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2-dichloro-1-(4-chlorophenyl)ethenyl]benzene
gaseous o,p-DDE number concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-p-DDEnumberconcentration
Number concentration means number of molecule per unit volume, and is used in the construction molecular_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chmical formula for o,p-DDE is C14H8Cl4. It is a member of the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2-dichloro-1-(4-chlorophenyl)ethenyl]benzene
gaseous o,p-DDT mass concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-p-DDTmassconcentration
Mass concentration means mass per unit volume and is used in the construction mass_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. The chmical formula for o,p-DDT is C14H9Cl5. It is a member of the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2,2-trichloro-1-(4-chlorophenyl)ethyl]benzene
pentanal and o-tolualdehyde mass concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/pentanalando-tolualdehydemassconcentration
Mass concentration means mass per unit volume and is used in the construction mass_concentration_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. Pentanal and o-tolualdehyde is a mixture of two compunds in the group of aldehydes.
precipitation o,p-DDT mass concentration - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/precipitationo-p-DDTmassconcentration
Mass concentration means mass per unit volume and is used in the construction mass_ concentration_ of_ X_ in_ Y, where X is a material constituent of Y. Precipitation is liquid or frozen water that forms in the atmosphere and falls to the earth. It comes in many forms, like rain, snow, and sleet. The chmical formula for o,p-DDT is C14H9Cl5. It belongs to the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2,2-trichloro-1-(4-chlorophenyl)ethyl]benzene
pentanal and o-tolualdehyde amount fraction - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/pentanalando-tolualdehydeamountfraction
Amount fraction is used in the construction mole_fraction_of_X_in_Y, where X is a material constituent of Y. A chemical species denoted by X may be described by a single term such as 'nitrogen' or a phrase such as 'nox_expressed_as_nitrogen'. Pentanal and o-tolualdehyde is a mixture of two compunds in the group of aldehydes.
gaseous o,p-DDT amount fraction - ACTRIS_VOCAB
https://vocabulary.actris.nilu.no/actris_vocab/o-p-DDTamountfraction
Amount fraction is used in the construction mole_fraction_of_X_in_Y, where X is a material constituent of Y. The chmical formula for o,p-DDT is C14H9Cl5. It is a member of the group of persistent organic pollutants (POPs). The IUPAC name is 1-chloro-2-[2,2,2-trichloro-1-(4-chlorophenyl)ethyl]benzene