COCC1OCC2O[Co]C3CC(O)=C(O)C(O)=C3c3c(O)c(O)c(O)cc3[Co]OC2[C@@H]1OC

InChIKey=DQLJTVMRVYIJHN-SDGKQJKISA-N

C20H24Co2O11

558.267

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Oxanes Monosaccharides Metal aryls Enediols Polyols Oxacyclic compounds Organic transition metal salts Metalloheterocyclic compounds Enols Dialkyl ethers Transition metal alkyls Organotransition metal compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Hydrolyzable tannin - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Metal aryl - Benzenoid - Oxane - Monosaccharide - Enediol - Oxacycle - Organic metal salt - Organic transition metal salt - Organoheterocyclic compound - Polyol - Metalloheterocycle - Ether - Enol - Dialkyl ether - Organic oxygen compound - Transition metal alkyl - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organometallic compound - Organic transition metal moeity - Aromatic heteropolycyclic 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