1365537-72-9

Upstream product

• 100-39-0 benzyl bromide 
• 39548-86-2 1‐(2‐(benzyloxy)‐4,6‐dihydroxyphenyl)ethan‐1‐one 
• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 
• 1365537-68-3 C₃₉H₃₈O₇ 
• 1365537-64-9 (2R)-5-benzyloxy-2-(4-benzyloxy-3-methoxyphenyl)-7-methoxymethoxychroman-3-one 
• 1365537-60-5 C₃₅H₃₆O₈ 
• 1365536-83-9 1-(2-(benzyloxy)-6-hydroxy-4-(methoxymethoxy)phenyl)ethan-1-one 
• 1365537-48-9 C₃₈H₄₆O₆Si 
• 1365537-40-1 C₃₂H₃₀O₇ 

Downstream Products

• 1421426-38-1 C₁₆H₁₆O₉S*H₃N 

Relevant academic research and scientific papers

Chemical synthesis and characterization of epicatechin glucuronides and sulfates: Bioanalytical standards for epicatechin metabolite identification

The monoglucuronides and sulfates of epicatechin, 3′- Omethylepicatechin, and 4′-O-methylepicatechin, respectively, were synthesized as authentic bioanalytical standards. Reversed-phase HPLC methods capable of baseline separation of the glucuronides and sulfates have been developed. Both the epicatechin glucuronides and sulfates were stable in the solid state when stored under ambient conditions and in aqueous solution when stored refrigerated. These results should prove invaluable to the research community as analytical standards as well as in future studies of the biological and pharmacological effects of epicatechin in humans.

A versatile approach to the regioselective synthesis of diverse (-)-epicatechin-β-d-glucuronides

A versatile new approach is reported for the total synthesis of five glucuronide metabolites of epicatechin, using selective protection/deprotection techniques.