1265877-23-3

Basic information

• Product Name: (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-(((S)-1-phenylallyl)amino)propanoate
• CAS NO: 1265877-23-3
• Molecular Weight: 334.415
• Mol File: 1265877-23-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-(((S)-1-phenylallyl)amino)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-(((S)-1-phenylallyl)amino)propanoate(1265877-23-3)
• EPA Substance Registry System: (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-(((S)-1-phenylallyl)amino)propanoate(1265877-23-3)

Safety Data

• Hazardous Substances Data: 1265877-23-3(Hazardous Substances Data)

Upstream product

• 264273-10-1 (S)-N(α)-tert-butyloxycarbonyl-N(β)-fluoren-9-ylmethyloxycarbonyl-2,3-diaminopropionic acid methyl ester 
• 131570-56-4 Boc-Dap(Fmoc)-OH 
• 76387-70-7 (S)-3-amino-2-tert-butoxycarbonylaminopropionic acid 
• 85217-69-2 cinnamyl methyl carbonate 
• 61040-20-8 (S)-methyl 3-amino-2-((tert-butoxycarbonyl)amino)propanoate 
• 104-54-1 3-Phenylpropenol 

Relevant articles and documents

Iridium-catalyzed asymmetric allylic amination with polar amines: Access to building blocks with lead-like molecular properties

The combination of an air-stable iridium catalyst and the dipolar aprotic solvent dimethyl sulfoxide (DMSO) allowed, for the first time, the systematic exploitation of highly polar, functionalized amines in asymmetric allylic substitutions: low molecular