Compounds containing a benzene ring conjugated to two methylidene groups at carbon atoms 1 and 2, respectively.

Terphenyls with a structure containing the 1,2-diphenylbenzene skeleton.

Organic compounds containing a benzene ring conjugated to a methylidene group and a ketone at carbon atoms 1 and 2, respectively.

Organic compounds containing a glycerone that carries an acyl substituent at the 1-position or the 2-position.

Quinones where the two C=O groups are attached at the 1- and 2-positions, respectively.

O-quinones that carry an imine group.

Benzoquinones where the two C=O groups are attached at the 1- and 2-positions, respectively.

Bromophenols carrying a iodine at the C2 position of the benzene ring.

Chlorophenols carrying a iodine at the C2 position of the benzene ring.

Fluorophenols carrying a iodine at the C2 position of the benzene ring.

Iodophenols carrying a iodine at the C2 position of the benzene ring.

Glucuronides in which the aglycone is linked to the carbohydrate unit through an O-glycosidic bond.

Quinonimines in which the imine groups are in a ortho-relationship.

Aromatic compounds that contain a o-xylene moiety, which is a monocyclic benzene carrying exactly two methyl groups at the 1- and 2-positions.

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.

Aromatic compounds containing a toluene, which carries a carboxamide group a the 2-position.

O-ester derivatives of thiocarbamic acid, with the general formula ROC(=S)NR2.

Compounds containing a pyrimidine , which is O-alkylated at one or more ring positions.

Hydroxylamines that are O-substituted with a phenyl group.

Phenols that are substituted with an amine group at the 2-position of the benzene ring.

Organic compounds containing an acetamide group conjugated to a phenyl group, which is in turn ortho-substituted with a halogen atom.

Aromatic compound containing a benzene ring which carries 2 amino groups, at the 1- and 2-positions.

Organic compounds containing a benzene ring fused to a 1,2-dioxin ring.

Compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.

Aurone flavonoids containing a carbohydrate moiety O-glycosidically bound to the aurone skeleton.

Compounds containing a carbohydrate moiety glycosidically linked to the rotenoid backbone at the C8-position.

Benzoic acids which bear a sulfanyl group (R-SH) attached to the benzene ring at positions 1 and 2, respectively.

Organic acids with the general formula RCO-SH (R=H, organic group).

Organic acids with the general formula RS(S)(=NH2)-OH (R=H, organic group).

Glycerone-3-phosphates carrying an alkyl substituent at the 1-position.

Glycerone-3-phosphates carrying an acyl substituent at the 1-position.

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.

Ester derivatives of carbothioic O-acids, with the general structure ROC(=S)R' where R = organyl group and R' = H or organyl group.

Cyclic organosulfur compounds with the general structure RC(=S)OR', R-R' = organyl group, where the central atom is part of the ring.

Ester derivatives of o-phthalic acids, which are based on a benzene 1,2-dicarboxylic acid skeleton.

Iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton.

Glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Organic compounds with the general formula HOS(R)(=N)(=S) (R = alkyl, aryl).

Organic acids with the general formula RS(=S)(=S)OH.

Flavonoids with methoxy groups conjugated to the flavonoid backbone.

Isoflavonoids with methoxy groups conjugated to the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.

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.

Isoflavones with methoxy groups attached to the C4' atom of the isoflavone backbone.

Isoflavones with methoxy groups attached to the C7 atom of the isoflavone backbone.

Flavones with methoxy groups attached to the C2' atom of the isoflavone backbone.

Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid.

O-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.

O-ester derivatives of dithiophosphates, with the general structure RSP(O)(O)=S (R = organyl group).

Glycerolipids containing a glycerol moiety that carries an alkyl group at the 1-position.

Organosulfur compounds with the general formula RS(O)(S)-OH.

Sulfonic acids with the general formula R-N-OS(O)(=O)=O. They can be synthesized through reaction of hydroxylamine and chlorosulfonic acids.

Benzofurans that a O-glycosylated at the 2-position. Benzofurans are organic compounds containing a benzene ring fused to a furan.

Benzofurans that a O-glycosylated at the 2-position. Benzofurans are organic compounds containing a benzene ring fused to a furan.

Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position.

Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid at the C3-position.

Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position.

Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid at the C7-position.

Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C8-position.

Phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid at the C8-position.

Phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C3'-position.

Phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C4'-position.

Phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C7-position.

Flavonoids with methoxy groups attached to the C2 atom of the flavonoid backbone.

Flavonoids with methoxy groups attached to the C3 atom of the flavonoid backbone.

Flavonoids with methoxy groups attached to the C4 atom of the flavonoid backbone.

Flavonoids with methoxy groups attached to the C5 atom of the flavonoid backbone.

Flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone.

Flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone.

Flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone.

Flavonoids with methoxy groups attached to the C2' atom of the flavonoid backbone.

Flavonoids with methoxy groups attached to the C3' atom of the flavonoid backbone.

Flavonoids with methoxy groups attached to the C4' atom of the flavonoid backbone.

Isoflavonoids with methoxy groups attached to the C2 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.

Isoflavonoids with methoxy groups attached to the C3 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.

Isoflavonoids with methoxy groups attached to the C4 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.

Isoflavonoids with methoxy groups attached to the C5 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.

Isoflavonoids with methoxy groups attached to the C6 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.

Isoflavonoids with methoxy groups attached to the C7 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.

Isoflavonoids with methoxy groups attached to the C8 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.

Isoflavonoids with methoxy groups attached to the C2' atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.

Isoflavonoids with methoxy groups attached to the C3' atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.

Isoflavonoids with methoxy groups attached to the C4' atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.

5-O-glycosylated neoflavonoids. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

7-O-glycosylated neoflavonoids. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

Phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C3-position.

Phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C5-position.

Hydroxylamines that are O-substituted with a phenyl group, and N-substituted by an alkyl group.

Organooxygen compounds that contain a phosphorodithioic acid, which is O-monosubstituted by an organyl group.

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.

Benzoic acid esters where the benzene ring is ortho-substituted with a hydroxy group.

Organic compounds containing a n-nitroso group -ON=O.

Compounds containing a O-glycosylated chalcone or dihydrochalcone moiety.

Benzoic acids (or derivatives) which bear a sulfanyl group (R-SH) attached to the benzene ring at positions 1 and 2, respectively.

Benzoic acids in which the hydrogen atom at position 2 of the benzene ring is replaced by a methoxy group.

Compounds containing a galloic acid moiety, linked to one hydroxyl group of a quinic acid moiety.

Compounds containing a benzene ring bearing a carboxylic acid group at ring carbon atoms 1 and 3.

Glycerolipids containing a chiral glycerol moiety that carries an alkyl group at the 1-position.

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.

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 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.

Flavonoid 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.

Flavonoid 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-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-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-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-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.

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.

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-cresol is C7H8O. It belongs to the group of aromatics. The IUPAC name is 2-methylphenol

Precipitation (tipping bucket gauge), Pronamic, Rain-O-Matic 400.042 - XX series (includes 400.042 - 10, 400.042 - 20, 400.042 - 25, 400.042 - 50. Also named Rain-O-Matic Meteorological Snow & Rain)