294181-78-5

Basic information

• Product Name: (2S,3R)-2-((R)-2-tert-Butoxycarbonylamino-2-methoxycarbonyl-propionylamino)-3-hydroxy-butyric acid benzyl ester
• Synonyms: (2S,3R)-2-((R)-2-tert-Butoxycarbonylamino-2-methoxycarbonyl-propionylamino)-3-hydroxy-butyric acid benzyl ester
• CAS NO: 294181-78-5
• Molecular Weight: 438.478
• Mol File: 294181-78-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3R)-2-((R)-2-tert-Butoxycarbonylamino-2-methoxycarbonyl-propionylamino)-3-hydroxy-butyric acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R)-2-((R)-2-tert-Butoxycarbonylamino-2-methoxycarbonyl-propionylamino)-3-hydroxy-butyric acid benzyl ester(294181-78-5)
• EPA Substance Registry System: (2S,3R)-2-((R)-2-tert-Butoxycarbonylamino-2-methoxycarbonyl-propionylamino)-3-hydroxy-butyric acid benzyl ester(294181-78-5)

Safety Data

• Hazardous Substances Data: 294181-78-5(Hazardous Substances Data)

Upstream product

• 150021-55-9 (R)-2-tert-Butoxycarbonylamino-2-methyl-malonic acid monomethyl ester 
• 150021-68-4 dimethyl 2-[(tert-butoxycarbonyl)amino]-2-methylmalonate 
• 24424-99-5 di-tert-butyl dicarbonate 
• 61172-70-1 dimethyl 2-(tert-butoxycarbonylamino)malonate 

Downstream Products

• 294181-89-8 2-((R)-1-{[2-((R)-1-{[2-((R)-1-tert-Butoxycarbonylamino-1-methoxycarbonyl-ethyl)-5-methyl-oxazole-4-carbonyl]-amino}-1-methoxycarbonyl-ethyl)-5-methyl-oxazole-4-carbonyl]-amino}-1-methoxycarbonyl-ethyl)-5-methyl-oxazole-4-carboxylic acid benzyl ester 
• 294181-87-6 2-((R)-1-{[2-((R)-1-tert-Butoxycarbonylamino-1-methoxycarbonyl-ethyl)-5-methyl-oxazole-4-carbonyl]-amino}-1-methoxycarbonyl-ethyl)-5-methyl-oxazole-4-carboxylic acid benzyl ester 
• 294181-80-9 2-(1-tert-butoxycarbonylamino-1-methoxycarbonyl-ethyl)-5-methyl-oxazole-4-carboxylic acid benzyl ester 

Relevant articles and documents

Synthesis of a second-generation pseudopeptide platform

A synthetic pathway is presented to a functionalized pseudopeptide molecular platform for use in supramolecular and solution-phase combinatorial chemistry. The platform contains amino acids with quaternary asymmetric centers, the configurations of which are determined by the method of synthesis. (C) 2000 Elsevier Science Ltd.