1365537-60-5

Basic information

• Product Name: C₃₅H₃₆O₈
• Synonyms: C₃₅H₃₆O₈
• CAS NO: 1365537-60-5
• Molecular Weight: 584.666
• Mol File: 1365537-60-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₃₅H₃₆O₈(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₅H₃₆O₈(1365537-60-5)
• EPA Substance Registry System: C₃₅H₃₆O₈(1365537-60-5)

Safety Data

• Hazardous Substances Data: 1365537-60-5(Hazardous Substances Data)

Upstream product

• 480-66-0 2,4,6-trihydroxyacetophenone 
• 115623-29-5 2-benzyloxy-4,6-bis(methoxymethyloxy)acetophenone 
• 65490-09-7 2'-hydroxy-4',6'-bis(methoxymethoxy)acetophenone 
• 1429227-36-0 (E)-{3-benzyloxy-2-[3-(4-benzyloxy-3-methoxyphenyl)allyl]-5-methoxymethoxyphenoxy}tert-butyldimethylsilane 
• 1429227-34-8 (E)-3-benzyloxy-2-[3-(3-benzyloxy-4-methoxyphenyl)allyl]-5-methoxymethoxyphenol 
• 1429227-33-7 (E)-1-(2-benzyloxy-6-hydroxy-4-methoxymethoxyphenyl)-3-(4-benzyloxy-3-methoxyphenyl)propenone 
• 39548-86-2 1‐(2‐(benzyloxy)‐4,6‐dihydroxyphenyl)ethan‐1‐one 
• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 
• 115-80-0 Triethyl orthopropionate 
• 1365537-53-6 (1S,2S)-3-[2-benzyloxy-6-(tert-butyl-dimethylsilanyloxy)-4-methoxymethoxyphenyl]-1-(4-benzyloxy-3-methoxyphenyl)propane-1,2-diol 
• 1365536-83-9 1-(2-(benzyloxy)-6-hydroxy-4-(methoxymethoxy)phenyl)ethan-1-one 
• 1365537-48-9 C₃₈H₄₆O₆Si 
• 1365537-40-1 C₃₂H₃₀O₇ 

Downstream Products

• 1365537-64-9 (2R)-5-benzyloxy-2-(4-benzyloxy-3-methoxyphenyl)-7-methoxymethoxychroman-3-one 
• 1365537-68-3 C₃₉H₃₈O₇ 
• 1365537-72-9 C₃₇H₃₄O₆ 

Relevant articles and documents

Enantioselective synthesis of orthogonally protected (2R,3R)-(-)- epicatechin derivatives, key intermediates in the de novo chemical synthesis of (-)-epicatechin glucuronides and sulfates

Ten orthogonally protected (-)-epicatechin and 3′- or 4′-O-methyl-(-)-epicatechin derivatives were prepared in a regiospecific and enantioselective manner. For each orthogonally protected (-)-epicatechin derivative, one specific phenolic hydroxyl was protected with a methoxymethyl (MOM) or p-methoxybenyzl (PMB) group and the remainder were protected as benzyl ethers. These uniquely protected (-)-epicatechin derivatives were designed to facilitate the regiospecific installation of a glucuronic acid or sulfate unit onto (-)-epicatechin after selective removal of the MOM or PMB protecting group to provide authentic standards of (-)-epicatechin glucuronides and sulfates.