56011-38-2

Basic information

• Product Name: 3-endo-benzyloxy-2-exo-bromobicyclo<3.2.0>heptan-6-one
• CAS NO: 56011-38-2
• Molecular Weight: 295.176
• Mol File: 56011-38-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-endo-benzyloxy-2-exo-bromobicyclo<3.2.0>heptan-6-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-endo-benzyloxy-2-exo-bromobicyclo<3.2.0>heptan-6-one(56011-38-2)
• EPA Substance Registry System: 3-endo-benzyloxy-2-exo-bromobicyclo<3.2.0>heptan-6-one(56011-38-2)

Safety Data

• Hazardous Substances Data: 56011-38-2(Hazardous Substances Data)

Upstream product

• 13173-09-6 bicyclo[3.2.0]hept-2-en-6-one 
• 100-51-6 benzyl alcohol 

Downstream Products

• 77426-16-5 15-epi-9-O-benzyl-prostaglandin-F₂α 
• 77426-16-5 (5Z,15S^*)-(+/-)-9α-benzyloxy-11α,15-dihydroxyprosta-5,13-dienoic acid 
• 77426-18-7 (Z)-7-[(1S,2S,5R)-5-Benzyloxy-2-((E)-(S)-3-hydroxy-oct-1-enyl)-3-oxo-cyclopentyl]-hept-5-enoic acid methyl ester 
• 77426-18-7 methyl (5Z,13E,15S^*)-(+/-)-9α-benzyloxy-15-hydroxy-11-oxoprosta-5,13-dienoate 
• 77426-20-1 methyl 15-epi-(13E,15S^*)-(+/-)-9α-benzyloxy-15-hydroxy-11-oxoprosta-13-enoate 
• 77426-20-1 methyl (13E,15S^*)-(+/-)-9α-benzyloxy-15-hydroxy-11-oxoprosta-13-enoate 
• 77426-10-9 (Z)-7-{(1S,2S,5R)-5-Benzyloxy-2-[(E)-3-(tert-butyl-dimethyl-silanyloxy)-oct-1-enyl]-3-oxo-cyclopentyl}-hept-5-enoic acid methyl ester 
• 77426-06-3 (5Z,13E)-(+/-)-9α-benzyloxy-15-(t-butyldimethylsilyloxy)-11α-hydroxyprosta-5,13-dienoic acid 
• 77426-11-0 (13E)-(+/-)-9α-benzyloxy-15-(t-butyldimethylsilyloxy)-11α-hydroxyprosta-13-enoic acid 
• 77426-14-3 {(1S,2S,3S,5R)-5-Benzyloxy-2-[(E)-3-(tert-butyl-dimethyl-silanyloxy)-oct-1-enyl]-3-hydroxy-cyclopentyl}-acetaldehyde 
• 64767-31-3 5-endo-benzyloxy-7-anti-<(E)-3-(t-butyldimethylsilyloxy)oct-1-enyl>bicyclo<2.2.1>heptan-2-one 
• 77426-09-6 (1S,5S,6R,8S)-6-Benzyloxy-8-((E)-3-hydroxy-oct-1-enyl)-2-oxa-bicyclo[3.2.1]octan-3-one 
• 64767-30-2 3-endo-benzyloxytricyclo<3.2.0.0^2,7>heptan-6-one 

Relevant articles and documents

Total Synthesis of Prostaglandin-F2α, and the 9-O-Benzyl Derivatives of Prostaglandins-F2α, -F1α, -D2, and -D1

As an extension of the method whereby prostaglandin-F2α may be prepared by homoconjugate addition of an organocuprate reagent to the 3-endo-silyloxytricyclo2,7>heptan-6-one (3), 3-endo-benzyloxytricyclo2,7