CCCC[Co]c1cc(O)c(O)c(O)c1C1=C(O)C(O)=C(CC1[Co]C)Oc1c(O)c(O)c(O)cc1C(O)=O

InChIKey=FGGVEVUVHJZAFT-UHFFFAOYSA-N

C24H26Co2O11

608.327

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

Gallic acids Pyrogallols and derivatives Benzoic acids Phenoxy compounds Benzoyl derivatives 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Metal aryls Polyols Organic transition metal salts Monocarboxylic acids and derivatives Enols Carboxylic acids Transition metal alkyls Organotransition metal compounds Organic oxides Hydrocarbon derivatives

Aromatic homomonocyclic compounds

Hydrolyzable tannin - Gallic acid - Gallic acid or derivatives - Hydroxybenzoic acid - Pyrogallol derivative - Benzoic acid - Benzoic acid or derivatives - Benzenetriol - Phenoxy compound - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Metal aryl - Benzenoid - Monocyclic benzene moiety - Organic transition metal salt - Polyol - Monocarboxylic acid or derivatives - Enol - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Transition metal alkyl - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organometallic compound - Organic transition metal moeity - 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) that 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