OCC1=CC=CC=C1O[C@@H]1O[C@H](COC(=O)\C=C\C2=CC=CC=C2)[C@@H](O)[C@H](O)[C@H]1O

InChIKey=JEPMPYQEMOEETI-YEINXZFXSA-N

C22H24O8

416.426

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Cinnamic acid esters O-glycosyl compounds Benzyl alcohols Styrenes Phenol ethers Phenoxy compounds Fatty acid esters Oxanes Monosaccharides Enoate esters Secondary alcohols Oxacyclic compounds Monocarboxylic acids and derivatives Acetals Polyols Organic oxides Hydrocarbon derivatives Aromatic alcohols Carbonyl compounds Primary alcohols

Aromatic heteromonocyclic compounds

Phenolic glycoside - Cinnamic acid or derivatives - Cinnamic acid ester - O-glycosyl compound - Phenoxy compound - Benzyl alcohol - Styrene - Phenol ether - Fatty acid ester - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Monosaccharide - Oxane - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Secondary alcohol - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Oxacycle - Acetal - Carboxylic acid derivative - Polyol - Alcohol - Aromatic alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - 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