289708-17-4

Basic information

• Product Name: {(S)-1-[(S)-1-(Butylcarbamoyl-hydroxy-methyl)-propylcarbamoyl]-3-methyl-butyl}-carbamic acid benzyl ester
• Synonyms: {(S)-1-[(S)-1-(Butylcarbamoyl-hydroxy-methyl)-propylcarbamoyl]-3-methyl-butyl}-carbamic acid benzyl ester
• CAS NO: 289708-17-4
• Molecular Weight: 435.564
• Mol File: 289708-17-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: {(S)-1-[(S)-1-(Butylcarbamoyl-hydroxy-methyl)-propylcarbamoyl]-3-methyl-butyl}-carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: {(S)-1-[(S)-1-(Butylcarbamoyl-hydroxy-methyl)-propylcarbamoyl]-3-methyl-butyl}-carbamic acid benzyl ester(289708-17-4)
• EPA Substance Registry System: {(S)-1-[(S)-1-(Butylcarbamoyl-hydroxy-methyl)-propylcarbamoyl]-3-methyl-butyl}-carbamic acid benzyl ester(289708-17-4)

Safety Data

• Hazardous Substances Data: 289708-17-4(Hazardous Substances Data)

Upstream product

• 153371-25-6 (2S)-2-(tert-butoxycarbonyl)aminobutyraldehyde 
• 2769-64-4 n-butyl isonitrile 
• 289707-96-6 (S)-2-Benzyloxycarbonylamino-4-methyl-pentanoic acid (S)-2-tert-butoxycarbonylamino-1-butylcarbamoyl-butyl ester 

Relevant articles and documents

Passerini multicomponent reaction of protected α-aminoaldehydes as a tool for combinatorial synthesis of enzyme inhibitors

Three-component Passerini condensation of N-Boc-α-aminoaldehydes with various isocyanides and carboxylic acids leads, after Boc- deprotection/transacylation, to complex peptide-like structures containing an α-hydroxy-β-aminoacid unit or, after oxidation,