78640-70-7

Upstream product

• 100-52-7 benzaldehyde 
• 1499-46-3 L-histidine methyl ester 
• 1499-46-3 L-Histidine methyl ester 

Downstream Products

• 69937-81-1 2-benzylamino-3-(3H-imidazol-4-yl)-propionic acid methyl ester 
• 1219090-51-3 N-methyl-L-hystidine methyl ester 
• 866392-18-9 N-benzyl-N-methyl-L-histidine methyl ester 
• 866392-27-0 N-(α-deuterobenzyl)-N-trideuteromethyl-L-histidine methyl ester 
• 69937-81-1 N-α-benzyl-L-histidine methyl ester 
• 866392-18-9 (S)-methyl 2-(benzyl(methyl)amino)-3-(1H-imidazol-4-yl)propanoate 
• 950758-74-4 methyl 2-(S)-[(benzyl)methylamino]-3-{1-[2-(methoxymethoxy)phenyl]-imidazol-4-yl}-propanoate 

Relevant academic research and scientific papers

Synthesis and structural characterization of cross-linked histidine-phenol Cu(II) complexes as cytochrome c oxidase active site models

Tridentate cross-linked histidine-phenol Cu(II) ether and ester complexes, chemical analogs of the active site of several heme-copper oxidases, have been synthesized and crystallized. The Royal Society of Chemistry.

Facile synthesis of highly functionalized N-methyl amino acid esters without side-chain protection

(Chemical Equation Presented) The facile, two-pot synthesis of N-methyl amino acid esters by way of reductive amination is presented. Side chain protection schemes are not required, the starting materials are all commercially available, and the synthetic