356570-63-3

Upstream product

• 586-75-4 4-chlorobenzoyl chloride 
• 356570-60-0 N-(4-bromobenzyl-1-carbonyl)-glycyl-glycine methyl ester 
• 138119-50-3 N-(4-bromobenzyl-1-carbonyl)-glycine methyl ester 
• 313958-35-9 N-(4-bromobenzyl-1-carbonyl)-glycyl-glycine 
• 5680-79-5 glycine ethyl ester hydrochloride 
• 18815-75-3 N-(4-bromobenzyl-1-carbonyl)-glycine 
• 586-76-5 4-Bromobenzoic acid 

Downstream Products

• 356570-64-4 N-(4-bromobenzyl-1-carbonyl)-glycyl-glycyl-glycine 
• 356570-67-7 N-(4-bromobenzyl-1-carbonyl)-glycyl-glycyl-glycyl-glycine methyl ester 
• 356570-68-8 N-(4-bromobenzyl-1-carbonyl)-glycyl-glycyl-glycyl-glycine 
• 356570-65-5 N-(4-bromobenzyl-1-carbonyl)-glycyl-glycyl-glycyl-tyrosine methyl ester 
• 356570-70-2 N-(4-bromobenzyl-1-carbonyl)-glycyl-glycyl-glycyl-glycyl-tyrosine methyl ester 

Relevant academic research and scientific papers

Synthesis and structural characterization of amino acid and peptide derivatives featuring N-(p-bromobenzoyl) substituents as promising connection unit for bio-inspired hybrid compounds

Using a sequence of activation, blocking and peptide coupling procedures, a series of ten amino acid and peptide derivatives 1-6 (a, b, respectively) featuring a p-bromobenzoyl substituent attached to the amino group of the parent compound has been synthe

Neutral peptide biradicals formed by dissociative electron transfer

(Matrix presented) A new method for the generation of transient neutral biradicals in liquid solution is reported. Photoinduced electron transfer in aqueous solution of the structures shown above leads to neutral biradicals with peptide spacers. Exchange