1054605-79-6

Basic information

• Product Name: (S)-5-Imidazol-1-yl-5-oxo-4-(trityl-amino)-pentanoic acid methyl ester
• CAS NO: 1054605-79-6
• Molecular Weight: 453.541
• Mol File: 1054605-79-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-5-Imidazol-1-yl-5-oxo-4-(trityl-amino)-pentanoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-5-Imidazol-1-yl-5-oxo-4-(trityl-amino)-pentanoic acid methyl ester(1054605-79-6)
• EPA Substance Registry System: (S)-5-Imidazol-1-yl-5-oxo-4-(trityl-amino)-pentanoic acid methyl ester(1054605-79-6)

Safety Data

• Hazardous Substances Data: 1054605-79-6(Hazardous Substances Data)

Upstream product

• 76-83-5 trityl chloride 
• 55878-80-3 N-trityl-L-glutamic acid 5-methyl ester 
• 530-62-1 1,1'-carbonyldiimidazole 
• 1499-55-4 L-glutamic acid 5-methyl ester 

Relevant articles and documents

Highly stereoselective syntheses of syn- and anti-1,2-amino alcohols

The reduction of N-protected amino ketones can be carried stereoselectively to produce either the syn- or anti-amino alcohol diastereomer. Carbamate-protected amino ketones can be reduced predictably and selectively to anti-amino alcohols with LiAlH(O-t-Bu)3 in ethanol at -78°C. N-Trityl-protected amino ketones can be reduced selectively to syn-amino alcohols with LiAlH(O-t-Bu)3 in THF at -5°C.