78393-95-0

Upstream product

• 154-23-4 catechin 
• 51079-25-5 (2R,3S)-(+)-catechin 3',4',5,7-tetramethyl ether 
• 77-78-1 dimethyl sulfate 
• 69119-42-2 3-O-benzyl-6,8-dibromo-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 186581-53-3 diazomethane 
• 88488-99-7 6-bromo-(+)-catechin 
• 78376-73-5 6,8-dibromo-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 69119-40-0 6-bromo-3',4',5,7-tetra-O-methyl-(+)-catechin 

Downstream Products

• 69119-50-2 8-bromo-3-O-acetyl-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 69119-52-4 8-hydroxy-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 69119-57-9 8-methoxycarbonyl-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 69119-54-6 8-acetoxy-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 69119-58-0 3-O-acetyl-8-methoxycarbonyl-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 69119-55-7 8-acetoxy-3-O-acetyl-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 69119-51-3 3-O-benzyl-8-hydroxy-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 28699-20-9 3-O-benzyl-8-bromo-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 69119-56-8 3-O-benzyl-8-methoxycarbonyl-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 69119-53-5 8-acetoxy-3-O-benzyl-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 99275-99-7 6-bromo-3,3',4',5,7-penta-O-methylcatechin 
• 23671-72-9 8-bromo-3',4',5,7-tetra-O-methyl-(+)-catechin 
• 51079-25-5 (2R,3S)-(+)-catechin 3',4',5,7-tetramethyl ether 
• 69119-43-3 6-bromo-3-O-acetyl-3',4',5,7-tetra-O-methyl-(+)-catechin 

Relevant academic research and scientific papers

Proton magnetic resonance spectra of catechin and bromocatechin derivatives: C6- vs. C8-substitution

The 1Hmr spectra of 20 catechin derivatives substituted at C-6/C-8 by bromine and/or hydrogen and at oxygen by methyl, acetyl, and/or hydrogen have been analyzed in deuterated acetone, acetonitrile, and chloroform.Because of its dependence on the nature o

Synthesis of Condensed Tannins. Part 12. Direct Access to - and -all-2,3-cis-Procyanidin Derivatives from (-)-Epicatechin: Assessment of Bonding Positions in Oligomeric Analogues from Crataegus oxyacantha L.

Synthesis of methyl ester acetates of - and -all-2,3-cis-procyanidin biflavanoids is effected by oxidative functionalization of (-)-epicatechin tetramethyl ester with lead tetra-acetate, and condensation of the resultant 2,3-cis-flavan-3,4-diol

Electrophilic Aromatic Substitution of Catechins: Bromination and Benzylation

Relative yields of C-6, C-8, and C-6 and C-8 substituted catechins obtained from the reaction of (+)-catechin or 3',4',5,7-tetra-O-methyl-(+)-catechin with pyridinium hydrobromide-perbromide, bromine, p-hydroxybenzyl alcohol, or o-hydroxybenzyl alcohol sh

Synthesis of Condensed Tannins. Part 3. Chemical Shifts for Determining the 6- and 8-Bonding Positions of 'Terminal' (+)-Catechin Units

Pairs of 6- and 8-functionalised (Br, OH, OAc, CO2Me, and CH2Me groups) 3',4',5,7-tetra-O-methyl-(+)-catechins available through selective bromination and debromination reactions and hence via lithio-analogues, provide diagnostic chemical shifts of their