151275-30-8

Basic information

• Product Name: (S)-1-((S)-2-tert-Butoxycarbonylamino-3-methoxycarbonyl-propionyl)-pyrrolidine-2-carboxylic acid benzyl ester
• CAS NO: 151275-30-8
• Molecular Weight: 434.489
• Mol File: 151275-30-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-1-((S)-2-tert-Butoxycarbonylamino-3-methoxycarbonyl-propionyl)-pyrrolidine-2-carboxylic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-((S)-2-tert-Butoxycarbonylamino-3-methoxycarbonyl-propionyl)-pyrrolidine-2-carboxylic acid benzyl ester(151275-30-8)
• EPA Substance Registry System: (S)-1-((S)-2-tert-Butoxycarbonylamino-3-methoxycarbonyl-propionyl)-pyrrolidine-2-carboxylic acid benzyl ester(151275-30-8)

Safety Data

• Hazardous Substances Data: 151275-30-8(Hazardous Substances Data)

Upstream product

• 16652-71-4 benzyl (2S)-2-pyrrolidinecarboxylate hydrochloride 
• 59768-74-0 (S)-2-t-butoxycarbonylaminosuccinic acid 4-methyl ester 

Downstream Products

• 151275-34-2 (S)-1-[(S)-3-Methoxycarbonyl-2-(2-propyl-pentanoylamino)-propionyl]-pyrrolidine-2-carboxylic acid benzyl ester 
• 769093-72-3 (S)-1-((S)-2-Amino-3-methoxycarbonyl-propionyl)-pyrrolidine-2-carboxylic acid benzyl ester 

Relevant articles and documents

Novel and general method for the preparation of peptidyl argininals

A general method for the synthesis of peptidyl argininals was developed which utilizes the novel building block N(g)-nitro-L-argininal ethyl aminal·HCl. The final aldehyde structure is generated by hydrolysis of the peptidic aminal moiety and can be applied to highly functionalized peptidic structures. The method is amenable to the preparation of large quantities of enantiomerically pure peptidyl argininals and was applied to the synthesis of two potent thrombin inhibitors.