71710-18-4

Basic information

• Product Name: N-(N-benzyloxycarbonyl-β-alanyl)-β-alanine ethyl ester
• Synonyms: N-(N-benzyloxycarbonyl-β-alanyl)-β-alanine ethyl ester
• CAS NO: 71710-18-4
• Molecular Weight: 322.361
• Mol File: 71710-18-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(N-benzyloxycarbonyl-β-alanyl)-β-alanine ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(N-benzyloxycarbonyl-β-alanyl)-β-alanine ethyl ester(71710-18-4)
• EPA Substance Registry System: N-(N-benzyloxycarbonyl-β-alanyl)-β-alanine ethyl ester(71710-18-4)

Safety Data

• Hazardous Substances Data: 71710-18-4(Hazardous Substances Data)

Upstream product

• 924-73-2 3-amino-propionic acid ethyl ester 
• 2304-94-1 3-(benzyloxycarbonylamino)propanoic acid 
• 4244-84-2 ethyl β-alaninate hydrochloride 
• 51513-97-4 N-[(phenylmethoxy)carbonyl]-β-alanine chloride 

Downstream Products

• 111196-05-5 (2-{2-[(S)-1-(4-Nitro-phenylcarbamoyl)-ethylcarbamoyl]-ethylcarbamoyl}-ethyl)-carbamic acid benzyl ester 
• 111196-11-3 3-carboxypropionyl-β-alanyl-β-alanyl-alanine p-nitroanilide 
• 69281-02-3 CbzβAlaβAla 
• 111196-13-5 N-(N-benzyloxycarbonyl-β-alanyl)-β-alanine hydrazide 

Relevant articles and documents

ROLE OF AMINO ACID RESIDUES IN CHROMOGENIC SUBSTRATES CLEAVED BY PANCREATIC ELASTASE

Anionic chromogenic substrates, 3-carboxypropionyl tripeptide p-nitroanilides modified with glycine, β-alanine, alanine, leucine, and proline in positions P1, P2, and P3 were synthesized.The substrates were digested with pancreatic elastase and the values of Km, kcat, and kcat/Km were determined.Alanine plays a decisive role in position P1, substrates with glycine or β-alanine in this position are not cleaved.The substitution in P2 is dominant for proline; next follow alanine, leucine, and glycine.The substitution in P3 is the least specific one.