CC(=O)C1=C(O)C=C(O)C=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChIKey=GFKQVLKFPJGJEP-RGCYKPLRSA-N

C14H18O9

330.289

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Alkyl-phenylketones Hexoses O-glycosyl compounds Acetophenones Resorcinols Phenoxy compounds Phenol ethers Aryl alkyl ketones Benzoyl derivatives 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Oxanes Vinylogous acids Secondary alcohols Polyols Acetals Oxacyclic compounds Primary alcohols Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - Alkyl-phenylketone - Hexose monosaccharide - O-glycosyl compound - Acetophenone - Phenylketone - Resorcinol - Aryl ketone - Aryl alkyl ketone - Phenol ether - Benzoyl - Phenoxy compound - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Oxane - Monocyclic benzene moiety - Monosaccharide - Vinylogous acid - Ketone - Secondary alcohol - Acetal - Organoheterocyclic compound - Oxacycle - Polyol - Organic oxide - Hydrocarbon derivative - 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