1380336-84-4

Basic information

• Product Name: methyl (S)-2-(((benzyloxy)carbonyl)amino)-3-(4-(4-chlorophenyl)-1H-1,2,3-triazol-1-yl)propanoate
• Synonyms: methyl (S)-2-(((benzyloxy)carbonyl)amino)-3-(4-(4-chlorophenyl)-1H-1,2,3-triazol-1-yl)propanoate
• CAS NO: 1380336-84-4
• Molecular Weight: 414.848
• Mol File: 1380336-84-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl (S)-2-(((benzyloxy)carbonyl)amino)-3-(4-(4-chlorophenyl)-1H-1,2,3-triazol-1-yl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (S)-2-(((benzyloxy)carbonyl)amino)-3-(4-(4-chlorophenyl)-1H-1,2,3-triazol-1-yl)propanoate(1380336-84-4)
• EPA Substance Registry System: methyl (S)-2-(((benzyloxy)carbonyl)amino)-3-(4-(4-chlorophenyl)-1H-1,2,3-triazol-1-yl)propanoate(1380336-84-4)

Safety Data

• Hazardous Substances Data: 1380336-84-4(Hazardous Substances Data)

Upstream product

• 873-73-4 4-n-chlorophenylacetylene 
• 1189196-22-2 (S)-3-benzyl 4-methyl 1,2,3-oxathiazolidine-3,4-dicarboxylate 2,2-dioxide 
• 1676-81-9 N-benzyloxycarbonyl-L-serine methyl ester 

Relevant articles and documents

Stereo- and regio-selective one-pot synthesis of triazole-based unnatural amino acids and β-amino triazoles

Synthesis of triazole based unnatural amino acids and β-amino triazoles has been described via a stereo and regioselective one-pot multi-component reaction of sulfamidates, sodium azide, and alkynes under MW conditions. The developed method is applicable to a broad substrate scope and has significant potential for the synthesis of unnatural amino acids with a triazole side chain.