911465-34-4

Basic information

• Product Name: ((E)-(R)-2,4-Diphenyl-but-3-enyl)-carbamic acid benzyl ester
• Synonyms: ((E)-(R)-2,4-Diphenyl-but-3-enyl)-carbamic acid benzyl ester
• CAS NO: 911465-34-4
• Molecular Weight: 357.452
• Mol File: 911465-34-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ((E)-(R)-2,4-Diphenyl-but-3-enyl)-carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: ((E)-(R)-2,4-Diphenyl-but-3-enyl)-carbamic acid benzyl ester(911465-34-4)
• EPA Substance Registry System: ((E)-(R)-2,4-Diphenyl-but-3-enyl)-carbamic acid benzyl ester(911465-34-4)

Safety Data

• Hazardous Substances Data: 911465-34-4(Hazardous Substances Data)

Upstream product

• 121440-71-9 ethyl (E)-1,3-diphenyl-2-propen-1-yl carbonate 
• 4663-33-6 1,3-diphenyl-3-hydroxypropene 
• 911676-21-6 C₁₆H₁₅NO₂ 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 430461-56-6 (R)-3-phenyl piperidine 
• 917810-87-8 Allyl-((E)-(R)-2,4-diphenyl-but-3-enyl)-carbamic acid benzyl ester 

Relevant articles and documents

Pd-catalyzed asymmetric allylic alkylation with nitromethane using a chiral diaminophosphine oxide: (S,RP)-Ph-DIAPHOX. Enantioselective synthesis of (R)-preclamol and (R)-baclofen

A Pd-catalyzed asymmetric allylic alkylation with nitromethane using an aspartic acid-derived P-chirogenic diaminophosphine oxide [(S,RP)-Ph-DIAPHOX] is described. This method was successfully applied to enantioselective synthesis of (R)-precla