890022-49-8

Basic information

• Product Name: {(R)-1-Benzyl-3-[(S)-2-((S)-1-tert-butylcarbamoyl-2-methyl-propylcarbamoyl)-pyrrolidin-1-yl]-1-[1,3]dithiolan-2-yl-propyl}-carbamic acid allyl ester
• Synonyms: {(R)-1-Benzyl-3-[(S)-2-((S)-1-tert-butylcarbamoyl-2-methyl-propylcarbamoyl)-pyrrolidin-1-yl]-1-[1,3]dithiolan-2-yl-propyl}-carbamic acid allyl ester
• CAS NO: 890022-49-8
• Molecular Weight: 604.879
• Mol File: 890022-49-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: {(R)-1-Benzyl-3-[(S)-2-((S)-1-tert-butylcarbamoyl-2-methyl-propylcarbamoyl)-pyrrolidin-1-yl]-1-[1,3]dithiolan-2-yl-propyl}-carbamic acid allyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: {(R)-1-Benzyl-3-[(S)-2-((S)-1-tert-butylcarbamoyl-2-methyl-propylcarbamoyl)-pyrrolidin-1-yl]-1-[1,3]dithiolan-2-yl-propyl}-carbamic acid allyl ester(890022-49-8)
• EPA Substance Registry System: {(R)-1-Benzyl-3-[(S)-2-((S)-1-tert-butylcarbamoyl-2-methyl-propylcarbamoyl)-pyrrolidin-1-yl]-1-[1,3]dithiolan-2-yl-propyl}-carbamic acid allyl ester(890022-49-8)

Safety Data

• Hazardous Substances Data: 890022-49-8(Hazardous Substances Data)

Upstream product

• 890022-44-3 4-benzyl-4-[2-(2-tert-butoxycarbonyl-pyrrolidin-1-yl)-ethyl]-2-tert-butyl-5-hydroxy-oxazolidine-3-carboxylic acid allyl ester 
• 890022-43-2 4-benzyl-4-[2-(2-tert-butoxycarbonyl-pyrrolidin-1-yl)-ethyl]-2-tert-butyl-5-oxo-oxazolidine-3-carboxylic acid allyl ester 
• 890022-42-1 (2S,4R)-4-Benzyl-4-(2-bromo-ethyl)-2-tert-butyl-5-oxo-oxazolidine-3-carboxylic acid allyl ester 
• 890022-45-4 (S)-1-((R)-3-Allyloxycarbonylamino-3-[1,3]dithiolan-2-yl-4-phenyl-butyl)-pyrrolidine-2-carboxylic acid 
• 3057-81-6 (S)-2-amino-N-tert-butyl-3-methylbutanamide 

Downstream Products

• 890022-55-6 (S)-1-((R)-3-Amino-3-[1,3]dithiolan-2-yl-4-phenyl-butyl)-pyrrolidine-2-carboxylic acid ((S)-1-tert-butylcarbamoyl-2-methyl-propyl)-amide 
• 890022-50-1 ((S)-1-{(R)-1-Benzyl-3-[(S)-2-((S)-1-tert-butylcarbamoyl-2-methyl-propylcarbamoyl)-pyrrolidin-1-yl]-1-[1,3]dithiolan-2-yl-propylcarbamoyl}-2-methyl-propyl)-carbamic acid benzyl ester 

Relevant articles and documents

An unusual functional group interaction and its potential to reproduce steric and electrostatic features of the transition states of peptidolysis

The donor-acceptor interaction between a tertiary amine and an aldehyde, first observed among a select class of alkaloids, was deliberately established in a peptidomimetic (1a-c) to mimic features of the two principal transition states of peptide hydrolys