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

InChIKey=OBEQZDSRAHQKEY-HTYBCISXSA-N

C20H23ClO6S

426.91

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Diphenylmethanes Hexoses C-glycosyl compounds Phenyl sulfoxides Chlorobenzenes Aryl chlorides Oxanes Sulfoxides 1,2-diols Secondary alcohols Sulfinyl compounds Oxacyclic compounds Dialkyl ethers Organochlorides Primary alcohols Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - Diphenylmethane - Hexose monosaccharide - C-glycosyl compound - Phenyl sulfoxide - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Oxane - Monosaccharide - 1,2-diol - Sulfoxide - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Sulfinyl compound - Dialkyl ether - Polyol - Ether - Primary alcohol - Hydrocarbon derivative - Organic oxide - Alcohol - Organosulfur compound - Organochloride - Organohalogen compound - 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