848047-71-2

Basic information

• Product Name: (2R,3S)-3,5,6,7,3',4'-hexa-O-benzylflavan
• Synonyms: (2R,3S)-3,5,6,7,3',4'-hexa-O-benzylflavan
• CAS NO: 848047-71-2
• Molecular Weight: 847.02
• Mol File: 848047-71-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3S)-3,5,6,7,3',4'-hexa-O-benzylflavan(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S)-3,5,6,7,3',4'-hexa-O-benzylflavan(848047-71-2)
• EPA Substance Registry System: (2R,3S)-3,5,6,7,3',4'-hexa-O-benzylflavan(848047-71-2)

Safety Data

• Hazardous Substances Data: 848047-71-2(Hazardous Substances Data)

Upstream product

• 917567-22-7 (2R,3S)-8-bromo-3,5,6,7,3',4'-hexa-O-benzylflavan 

Downstream Products

• 917567-28-3 (2R,3S)-3,5,6,7,3',4'-hexahydroxyflavan 

Relevant articles and documents

Hydroxylation of ring A of flavan-3-ols: Influence of the ring A substitution pattern on the oxidative rearrangement of 6-hydroxyflavan-3-ols

A general procedure for the oxidation of catechin derivatives is described, leading to the introduction of a new hydroxyl group at C-6. This procedure has been used for the synthesis of a number of 6-hydroxy flavan-3-ols, including elephantorrhizol, a natural flavan-3-ol exhibiting a fully substituted A ring. The substitution at C-8, albeit of poor influence on the course of this oxidation reaction, has been demonstrated to be preponderant for the further spontaneous oxidation and rearrangement of 6-hydroxy-flavan-3-ols into p-benzoquinones. The whole procedure allows the preparation of 6-alkyl substituted benzoquinones derived from catechin. Georg Thieme Verlag Stuttgart.