COC1=C(O)C=CC(=C1)C(=O)OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey=VLDUXRGYOUFMGC-GRJWACCOSA-N

C14H18O9

330.289

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

p-Hydroxybenzoic acid alkyl esters M-methoxybenzoic acids and derivatives Methoxyphenols Anisoles Benzoyl derivatives Methoxybenzenes Phenoxy compounds Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Monosaccharides Oxanes 1,2-diols Secondary alcohols Hemiacetals Carboxylic acid esters Oxacyclic compounds Hydrocarbon derivatives Organic oxides

Aromatic heteromonocyclic compounds

Hydrolyzable tannin - P-hydroxybenzoic acid alkyl ester - P-hydroxybenzoic acid ester - M-methoxybenzoic acid or derivatives - Benzoate ester - Methoxyphenol - Benzoic acid or derivatives - Anisole - Phenoxy compound - Benzoyl - Phenol ether - Methoxybenzene - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Monosaccharide - Oxane - Hemiacetal - Carboxylic acid ester - 1,2-diol - Secondary alcohol - Ether - Carboxylic acid derivative - Polyol - Organoheterocyclic compound - Oxacycle - Organic oxide - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - Aromatic heteromonocyclic 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