155518-27-7

Basic information

• Product Name: N^α-tert-butoxycarbonyl-L-alanyl-L-alanyl-L-alanyl-(N^ε-benzyloxycarbonyl)-L-lysyl-L-alanyl-(N^ε-(benzo-18-crown-6)-4-carbonyl)-L-lysyl-L-alanine methyl ester
• CAS NO: 155518-27-7
• Molecular Weight: 1216.39
• Mol File: 155518-27-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N^α-tert-butoxycarbonyl-L-alanyl-L-alanyl-L-alanyl-(N^ε-benzyloxycarbonyl)-L-lysyl-L-alanyl-(N^ε-(benzo-18-crown-6)-4-carbonyl)-L-lysyl-L-alanine methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N^α-tert-butoxycarbonyl-L-alanyl-L-alanyl-L-alanyl-(N^ε-benzyloxycarbonyl)-L-lysyl-L-alanyl-(N^ε-(benzo-18-crown-6)-4-carbonyl)-L-lysyl-L-alanine methyl ester(155518-27-7)
• EPA Substance Registry System: N^α-tert-butoxycarbonyl-L-alanyl-L-alanyl-L-alanyl-(N^ε-benzyloxycarbonyl)-L-lysyl-L-alanyl-(N^ε-(benzo-18-crown-6)-4-carbonyl)-L-lysyl-L-alanine methyl ester(155518-27-7)

Safety Data

• Hazardous Substances Data: 155518-27-7(Hazardous Substances Data)

Upstream product

• 27317-70-0 N^α-tert-butoxycarbonyl-L-alanyl-L-alanyl-L-alanine 
• 27317-69-7 N-tert-butoxycarbonyl-L-alanyl-L-alanine 
• 19794-10-6 (S)-methyl 2-((S)-2-((tert-butoxycarbonyl)amino)propanamido)propanoate 
• 2389-45-9 Boc-Lys(Z)-OH 
• 155479-37-1 N^α-tert-butoxycarbonyl-(N^ε-benzyloxycarbonyl)-L-lysyl-L-alanyl-(N^ε-(benzo-18-crown-6)-4-carbonyl)-L-lysyl-L-alanine methyl ester 
• 155479-35-9 N^α-tert-butoxycarbonyl-L-alanyl-(N^ε-(benzo-18-crown-6)-4-carbonyl)-L-lysyl-L-alanine methyl ester 
• 155479-34-8 N^α-tert-butoxycarbonyl-L-alanyl-L-lysyl-L-alanine methyl ester 
• 27909-29-1 N^α-tert-butoxycarbonyl-L-alanyl-(N^ε-benzyloxy-carbonyl)-L-lysyl-L-alanine methyl ester 
• 22839-06-1 Boc-Lys(Z)-Ala-OMe 
• 19963-33-8 N^α-tert-butoxycarbonyl-L-alanyl-L-alanyl-L-alanine methyl ester 

Relevant articles and documents

Design and Synthesis of Novel Peptides Bearing a Host and a Guest Side Chains

The synthesis of model heptapeptides bearing a host and a guest side chains at different positions is reported.These peptide structures were designated in such a way that specific backbone conformations could be induced and stabilized by cooperative side