O[C@@H]1[C@@H](O)[C@H](OC2=CC=C(C=C2)C(=C\Cl)\C2=CC=C(O)C=C2)O[C@@H]([C@H]1O)C(O)=O

InChIKey=XISRFPSBCZDHKG-BBGXLIRQSA-N

C20H19ClO8

422.81

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Fatty acyl glycosides of mono- and disaccharides O-glucuronides Diphenylmethanes Alkyl glycosides Hexoses O-glycosyl compounds Styrenes Phenoxy compounds Phenol ethers 1-hydroxy-2-unsubstituted benzenoids Beta hydroxy acids and derivatives Pyrans Oxanes Secondary alcohols Acetals Polyols Monocarboxylic acids and derivatives Chloroalkenes Carboxylic acids Oxacyclic compounds Vinyl chlorides Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteromonocyclic compounds

Phenolic glycoside - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - 1-o-glucuronide - O-glucuronide - Diphenylmethane - Glucuronic acid or derivatives - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - Phenoxy compound - Styrene - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - Beta-hydroxy acid - Phenol - Monocyclic benzene moiety - Fatty acyl - Hydroxy acid - Monosaccharide - Benzenoid - Oxane - Pyran - Secondary alcohol - Polyol - Vinyl halide - Vinyl chloride - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Chloroalkene - Acetal - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Haloalkene - Carbonyl group - Hydrocarbon derivative - Organochloride - Organic oxide - Organohalogen compound - Alcohol - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Not available