CC[Si](CC)(CC)OC1=C(O[Si](CC)(CC)CC)C(O[Si](CC)(CC)CC)=C2OC3=C(OC2=C1)C1=C2C(=C3)C(=O)OC3=C2C(=CC(O[Si](CC)(CC)CC)=C3O[Si](CC)(CC)CC)C(=O)O1

InChIKey=XLZHAHVLQHLXLV-UHFFFAOYSA-N

C50H78O11Si5

995.588

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

Ellagic acids and derivatives Isocoumarins and derivatives Coumarins and derivatives 2-benzopyrans 1-benzopyrans Pyranones and derivatives Trialkylheterosilanes Heteroaromatic compounds Lactones Oxacyclic compounds Organic metalloid salts Organooxygen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Hydrolyzable tannin - Ellagic_acid - Coumarin - Isocoumarin - Benzopyran - 1-benzopyran - 2-benzopyran - Pyranone - Pyran - Benzenoid - Trialkylheterosilane - Heteroaromatic compound - Lactone - Oxacycle - Organoheterosilane - Organic metalloid salt - Organoheterocyclic compound - Organosilicon compound - Organic oxygen compound - Organooxygen compound - Organic metalloid moeity - Hydrocarbon derivative - Organic oxide - 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) 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