CCOC1=CC=C(CC2=C(Cl)C=CC(=C2)C2(O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1

InChIKey=KYDGWGYAUCJZDV-AWGDKMGJSA-N

C21H25ClO7

424.87

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Diphenylmethanes Hexoses Phenoxy compounds Phenol ethers Chlorobenzenes Alkyl aryl ethers Oxanes Aryl chlorides Secondary alcohols Hemiacetals 1,2-diols Oxacyclic compounds Primary alcohols Organochlorides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - Diphenylmethane - Hexose monosaccharide - Phenoxy compound - Phenol ether - Alkyl aryl ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Oxane - Secondary alcohol - Hemiacetal - 1,2-diol - Ether - Organoheterocyclic compound - Oxacycle - Polyol - Hydrocarbon derivative - Organohalogen compound - Organochloride - Alcohol - Primary 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