106561-18-6

Basic information

• Product Name: N-(benzyloxycarbonyl)-L-leucyl-L-leucyl-L-leucine methyl ester
• CAS NO: 106561-18-6
• Molecular Weight: 505.655
• Mol File: 106561-18-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(benzyloxycarbonyl)-L-leucyl-L-leucyl-L-leucine methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(benzyloxycarbonyl)-L-leucyl-L-leucyl-L-leucine methyl ester(106561-18-6)
• EPA Substance Registry System: N-(benzyloxycarbonyl)-L-leucyl-L-leucyl-L-leucine methyl ester(106561-18-6)

Safety Data

• Hazardous Substances Data: 106561-18-6(Hazardous Substances Data)

Upstream product

• 2018-66-8 Z-Leu-OH 
• 6491-83-4 ((S)-2-amino-4-methylpentanoyl)-L-leucine methyl ester hydrochloride 
• 15136-13-7 N-tert-butoxycarbonyl-L-leucyl-L-leucine methyl ester 
• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 
• 7517-19-3 methyl (L)-leucinate hydrochloride 
• 3504-37-8 Cbz-L-Leu-L-Leu-OMe 
• 7801-71-0 N-benzyloxycarbonyl-L-leucyl-L-leucine 

Downstream Products

• 18867-97-5 carbobenzoxy-L-leucyl-L-leucyl-L-leucine 
• 98695-41-1 N-carbobenzoxy-L-leucyl-L-leucyl-L-leucyl-L-leucyl-L-leucine methyl ester 

Relevant articles and documents

Chloride-Assisted Peptide Macrocyclization

The role of the Cl- anion as a templating agent for the synthesis of cyclopeptides was assessed through the preparation of three new homocyclolysines and other six cyclic peptides by head-to-tail lactamization. Isolated yields of products obtai

Recyclable hypervalent iodine(III) reagent iodosodilactone as an efficient coupling reagent for direct esterification, amidation, and peptide coupling

A hypervalent iodine(III) reagent plays a novel role as an efficient coupling reagent to promote the direct condensation between carboxylic acids and alcohols or amines to provide esters, macrocyclic lactones, amides, as well as peptides without racemization. The regeneration of iodosodilactone (1) can also be readily achieved. The intermediate acyloxyphosphonium ion C from the activation of a carboxylic acid is thought to be involved in the present esterification reaction.