628298-45-3

Upstream product

• 298-12-4 Glyoxilic acid 
• 403739-55-9 rac-1-(4-methoxyphenyl)-2-(4-methylbenzylsulfanyl)ethylamine 
• 628298-43-1 1-(4-methoxyphenyl)-2-(4-methylbenzylsulfanyl)ethanol 
• 628298-41-9 thioacetic acid S-(4-methylbenzyl) ester 
• 104-82-5 4-Methylbenzyl chloride 
• 403739-54-8 1-(4-methoxyphenyl)-2-(4-methylbenzylsulfanyl)ethanone 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 4498-99-1 4-methylbenzylthiol 
• 821785-31-3 1-(4-methoxyphenyl)-2-(4-methylbenzylsulfanyl)ethanone O-methyloxime 
• 628298-44-2 rac-[1-(4-methoxyphenyl)-2-(4-methylbenzylsulfanyl)ethylamino]acetic acid ethyl ester 

Downstream Products

• 628298-46-4 [[1-(4-methoxyphenyl)-2-(4-methylbenzylsulfanyl)ethyl](2,2,2-trichloroethoxycarbonyl)amino]acetic acid 
• 821785-37-9 C₅₁H₇₁N₁₁O₁₃S₂ 
• 821785-41-5 rac-[4-(4-methoxyphenyl)thiazolidin-3-yl]acetic acid 
• 821785-43-7 3-((S)-2-{(S)-4-Carbamoyl-2-[(S)-2-(2-{2-[4-(4-methoxy-phenyl)-thiazolidin-3-yl]-acetylamino}-acetylamino)-propionylamino]-butyrylamino}-3-phenyl-propionylamino)-propionic acid 
• 821785-45-9 N-(3-{(2S,5S,17S,20S)-5-Benzyl-20-(4-hydroxy-benzyl)-17-hydroxymethyl-10-[2-mercapto-1-(4-methoxy-phenyl)-ethyl]-3,6,9,12,15,18,21-heptaoxo-1,4,7,10,13,16,19-heptaaza-cyclohenicos-2-yl}-propyl)-guanidine 
• 628298-47-5 [[(benzylcarbamoylmethyl)carbamoyl]methyl][1-(4-methoxyphenyl)-2-(4-methylbenzylsulfanyl)ethyl]carbamic acid 2,2,2-trichloroethyl ester 

Relevant academic research and scientific papers

Synthesis of nα-(1-phenyl-2-mercaptoethyl) amino acids, new building blocks for ligation and cyclization at non-cysteine sites: Scope and limitations in peptide synthesis

A new and convenient method for the synthesis and incorporation of N α-(1-phenyl-2-mercaptoethyl)-derivatized amino acids applicable to chemical ligation at non-cysteine sites is presented. Nα- Auxiliary derivatives of glycine and al

Derivatized Amino Acids Relevant to Native Peptide Synthesis by Chemical Ligation and Acyl Transfer

Three amino acids were converted into the derivatives 5.2 (from glycine), 6.4a and 6.4b (from alanine), and 8.3a and 8.3b (from O-benzyl serine). These N-alkylated amino acids, which can be deprotected after conversion of the carboxyl into an amide, correspond to the general structure 2.1, a compound class of use in the study of peptide segment coupling by the ligation-acyl transfer method.