OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)C1=CC(CC2=CC=C(OC(F)F)C=C2)=C(Cl)C=C1

InChIKey=WUNBGSKGXHOUHI-FQBWVUSXSA-N

C20H21ClF2O6

430.83

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Diphenylmethanes Hexoses C-glycosyl compounds Phenoxy compounds Phenol ethers Chlorobenzenes Aryl chlorides Oxanes Secondary alcohols 1,2-diols Oxacyclic compounds Dialkyl ethers Hydrocarbon derivatives Alkyl fluorides Primary alcohols Organochlorides Organofluorides

Aromatic heteromonocyclic compounds

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