76567-06-1

Basic information

• Product Name: cis-1-carbobenzyloxy-2-methyl-3-(N-p-tolyl)amidoaziridine
• Synonyms: cis-1-carbobenzyloxy-2-methyl-3-(N-p-tolyl)amidoaziridine
• CAS NO: 76567-06-1
• Molecular Weight: 324.379
• Mol File: 76567-06-1.mol

Chemical Properties

• CAS DataBase Reference: cis-1-carbobenzyloxy-2-methyl-3-(N-p-tolyl)amidoaziridine(CAS DataBase Reference)
• NIST Chemistry Reference: cis-1-carbobenzyloxy-2-methyl-3-(N-p-tolyl)amidoaziridine(76567-06-1)
• EPA Substance Registry System: cis-1-carbobenzyloxy-2-methyl-3-(N-p-tolyl)amidoaziridine(76567-06-1)

Safety Data

• Hazardous Substances Data: 76567-06-1(Hazardous Substances Data)

Upstream product

• 106-49-0 p-toluidine 
• 19728-63-3 N-benzyloxycarbonyl-L-treonine 
• 76567-05-0 ((1S,2R)-2-Hydroxy-1-p-tolylcarbamoyl-propyl)-carbamic acid benzyl ester 
• 76567-05-0 ((R)-2-Hydroxy-1-p-tolylcarbamoyl-propyl)-carbamic acid benzyl ester 

Relevant articles and documents

Stereoselective chiral synthesis of N-aryl-α-amino-β-lactams from β-hydroxy-α-amino acids

Arylamides of amino-protected β-hydroxy-α-amino acids were cyclized to optically pure, cis- or trans-3-amino-1-aryl-2-azetidinone derivatives by an intramolecular SN2 reaction mediated by diethyl azodicarboxylate and triphenylphosphine or hexamethylphosphorus triamide.