159425-56-6

Basic information

• Product Name: 1,1-dimethylethyl 4-<<2-(benzyloxy)-6-(1,3-dioxanyl)phenyl>hydroxymethyl>-3,5-bis(benzyloxy)benzoate
• Synonyms: 1,1-dimethylethyl 4-<<2-(benzyloxy)-6-(1,3-dioxanyl)phenyl>hydroxymethyl>-3,5-bis(benzyloxy)benzoate
• CAS NO: 159425-56-6
• Molecular Weight: 688.818
• Mol File: 159425-56-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,1-dimethylethyl 4-<<2-(benzyloxy)-6-(1,3-dioxanyl)phenyl>hydroxymethyl>-3,5-bis(benzyloxy)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-dimethylethyl 4-<<2-(benzyloxy)-6-(1,3-dioxanyl)phenyl>hydroxymethyl>-3,5-bis(benzyloxy)benzoate(159425-56-6)
• EPA Substance Registry System: 1,1-dimethylethyl 4-<<2-(benzyloxy)-6-(1,3-dioxanyl)phenyl>hydroxymethyl>-3,5-bis(benzyloxy)benzoate(159425-56-6)

Safety Data

• Hazardous Substances Data: 159425-56-6(Hazardous Substances Data)

Upstream product

• 158584-99-7 3-(benzyloxy)-2-bromobenzaldehyde 
• 159425-38-4 2-<2-bromo-3-(benzyloxy)phenyl>-1,3-dioxane 
• 158585-00-3 2-bromo-3-benzyloxy-benzyl alcohol 
• 1700-30-7 (3-(benzyloxy)phenyl)methanol 
• 159425-55-5 2-<2-formyl-3-(benzyloxy)phenyl>-1,3-dioxane 
• 158980-57-5 3,5-dibenzyloxy-4-bromobenzoic acid tert-butyl ester 

Downstream Products

• 159425-58-8 3,5-bis(benzyloxy)-4-<2-(benzyloxy)-6-(1,3-dioxanyl)benzoyl>benzoic acid 
• 158980-63-3 1,1-dimethylethyl 4-<6-(benzyloxy)-2-<(benzyloxy)carbonyl>benzoyl>-3,5-bis(benzyloxy)benzoate 
• 158585-06-9 4-(6-Benzyloxy-2-(benzyloxycarbonyl)benzoyl)-3,5-dibenzyloxybenzoic Acid 
• 158980-62-2 3-Benzyloxy-2-[2,6-dibenzyloxy-4-(1,1-dimethylethoxycarbonyl)-benzoyl]benzoic acid 
• 158980-61-1 1,1-dimethylethyl 3,5-bis(benzyloxy)-4-<6-(benzyloxy)-2-formylbenzoyl>benzoate 
• 159425-57-7 1,1-dimethylethyl 4-<2-(benzyloxy)-6-(1,3-dioxanyl)benzoyl>-3,5-bis(benzyloxy)benzoate 

Relevant articles and documents

Total synthesis of balanol, part 2. Completion of the synthesis and investigation of the structure and reactivity of two key heterocyclic intermediates

A convergent enantioselective total synthesis of the natural product (-)-balanol (1) is described. In addition to benzophenone fragment 8, key intermediates are chiral bicyclic aziridine 3 and the corresponding epoxide 4, both of which undergo highly regi