OC(C1=CC=C(O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O)C=C1)C1=C(Cl)C=C(Cl)C=C1

InChIKey=UPAWZCAHYAYBEU-KLUKMEKLSA-N

C18H18Cl2O6

401.24

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Diphenylmethanes O-glycosyl compounds Pentoses Phenoxy compounds Phenol ethers Dichlorobenzenes Oxanes Aryl chlorides Secondary alcohols Polyols Oxacyclic compounds Acetals Organochlorides Hydrocarbon derivatives Aromatic alcohols

Aromatic heteromonocyclic compounds

Phenolic glycoside - Diphenylmethane - O-glycosyl compound - Pentose monosaccharide - 1,3-dichlorobenzene - Phenoxy compound - Phenol ether - Chlorobenzene - Halobenzene - Oxane - Aryl halide - Monocyclic benzene moiety - Monosaccharide - Aryl chloride - Benzenoid - Secondary alcohol - Polyol - Oxacycle - Acetal - Organoheterocyclic compound - Hydrocarbon derivative - Organohalogen compound - Organochloride - Aromatic alcohol - 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