150074-36-5

Basic information

• Product Name: [(S)-1-((S)-1-Methyl-2,3-dioxo-propylcarbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester
• Synonyms: [(S)-1-((S)-1-Methyl-2,3-dioxo-propylcarbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester
• CAS NO: 150074-36-5
• Molecular Weight: 382.416
• Mol File: 150074-36-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: [(S)-1-((S)-1-Methyl-2,3-dioxo-propylcarbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(S)-1-((S)-1-Methyl-2,3-dioxo-propylcarbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester(150074-36-5)
• EPA Substance Registry System: [(S)-1-((S)-1-Methyl-2,3-dioxo-propylcarbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester(150074-36-5)

Safety Data

• Hazardous Substances Data: 150074-36-5(Hazardous Substances Data)

Upstream product

• 3338-39-4 N-benzyloxycarbonyl-L-phenylalanyl-L-alanine 
• 71732-53-1 (Z,3S)-1-diazonio-3-[[(2S)-3-phenyl-2-(phenylmethoxycarbonylamino)propanoyl]amino]but-1-en-2-olate carbamic acid 

Relevant articles and documents

Synthesis of amino acid-derived imidazoles from enantiopure N-protected α-amino glyoxals

A range of novel imidazoles, including three histidine derivatives, with chiral side chains derived from amino acids and dipeptides have been synthesised from N-Cbz-protected α-amino glyoxals. (C) 2000 Elsevier Science Ltd.