COC(=O)C1=CC(OC)=C(O)C(O)=C1C1=C(O)C(O)=C(OC)C=C1C(=O)OC

InChIKey=QMASVVWOCXFGJB-UHFFFAOYSA-N

C18H18O10

394.332

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

Biphenols Gallic acid and derivatives Biphenyls and derivatives p-Hydroxybenzoic acid alkyl esters m-Hydroxybenzoic acid esters M-methoxybenzoic acids and derivatives Methoxyphenols Phenoxy compounds Methoxybenzenes Anisoles Catechols Benzoyl derivatives 1-hydroxy-4-unsubstituted benzenoids Alkyl aryl ethers Methyl esters Organic oxides Hydrocarbon derivatives

Aromatic homomonocyclic compounds

Hydrolyzable tannin - Biphenol - Biphenyl - Gallic acid or derivatives - P-hydroxybenzoic acid alkyl ester - M-hydroxybenzoic acid ester - P-hydroxybenzoic acid ester - Dihydroxybenzoic acid - M-methoxybenzoic acid or derivatives - Benzoate ester - Methoxyphenol - Benzoic acid or derivatives - Phenol ether - Methoxybenzene - Benzoyl - Phenoxy compound - Anisole - Catechol - Phenol - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Methyl ester - Carboxylic acid ester - Ether - Carboxylic acid derivative - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound

This compound belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Not available