917810-87-8

Basic information

• Product Name: Allyl-((E)-(R)-2,4-diphenyl-but-3-enyl)-carbamic acid benzyl ester
• Synonyms: Allyl-((E)-(R)-2,4-diphenyl-but-3-enyl)-carbamic acid benzyl ester
• CAS NO: 917810-87-8
• Molecular Weight: 397.517
• Mol File: 917810-87-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Allyl-((E)-(R)-2,4-diphenyl-but-3-enyl)-carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Allyl-((E)-(R)-2,4-diphenyl-but-3-enyl)-carbamic acid benzyl ester(917810-87-8)
• EPA Substance Registry System: Allyl-((E)-(R)-2,4-diphenyl-but-3-enyl)-carbamic acid benzyl ester(917810-87-8)

Safety Data

• Hazardous Substances Data: 917810-87-8(Hazardous Substances Data)

Upstream product

• 4663-33-6 1,3-diphenyl-3-hydroxypropene 
• 121440-71-9 ethyl (E)-1,3-diphenyl-2-propen-1-yl carbonate 
• 501-53-1 benzyl chloroformate 
• 911676-21-6 C₁₆H₁₅NO₂ 
• 911465-34-4 ((E)-(R)-2,4-Diphenyl-but-3-enyl)-carbamic acid benzyl ester 
• 106-95-6 allyl bromide 

Downstream Products

• 430461-56-6 (R)-3-phenyl piperidine 

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