17350-66-2

Upstream product

• 28819-05-8 (S)-2-benzyloxycarbonylamino-propionic acid methyl ester 
• 501-53-1 benzyl chloroformate 
• 60625-90-3 Cbz-alanine ethyl ester 

Downstream Products

• 79458-92-7 N-(Benzyloxycarbonyl-L-ananyl)-L-histidine 
• 28416-91-3 (S)-benzyl (1-azido-1-oxopropan-2-yl)carbamate 
• 3253-17-6 α-N(L-alanyl)-histidine 
• 287728-93-2 [(S)-1-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylcarbamoyl)-ethyl]-carbamic acid benzyl ester 
• 87023-87-8 1-(Cbz-alanyl)-3,5-dimethylpyrazole 
• 94068-22-1 N,N'-bis(benzyloxycarbonyl)ethane-1,1-diamine 
• 64789-41-9 N-benzyloxycarbonyl-N'-t-butyloxycarbonylethane-1,1-diamine 
• 102195-74-4 N,N'-bis(1-benzyloxycarbonylaminoethyl)urea 
• 88491-33-2 (S)-N-benzyloxycarbonyl-N'-ethoxycarbonylethane-1,1-diamine 
• 1310714-71-6 Cbz-L-Ala-HdHz 
• 1352815-87-2 C₂₃H₁₉N₃O₅ 
• 58651-28-8 benzyloxycarbonylalanyl-glycine hydrazide 
• 3057-56-5 Cbz-alanylglycylglycyl hydrazide 
• 3057-63-4 Cbz-alanylglycylglycine ethyl ester 

Relevant academic research and scientific papers

A favorable, narrow, δh Hansen-parameter domain for gelation of low-molecular-weight amino acid derivatives

In recent years, the design of new low-molecular-weight gelators (LMWGs) has attracted considerable attention because of the interesting supramolecular architectures as well as industrial applications. In this context, the role of the organic solvent in d

Self-assembly and mechanism of L-Alanine-based dihydrazide derivative as excellent gelator of organic solvents

A new organogelator, L-Alanine dihydrazide derivative can self-assemble in various organic solvents and turned them into thermally reversible physical supramolecular organogels at extremely low concentrations ( 2 wt %). The gel-sol phase transition tempe

Combinatorial synthesis of 3,5-Dimethylene substituted 1,2,4-Triazoles

Combinatorial cyclizations of imidates and hydrazides with methylene linked R groups, generated from the corresponding nitriles and carboxylic acids, respectively, provided a large library of 3,5-dimethylene substituted 1,2,4- trizoles. 2011 Bentham Science Publishers Ltd.

New system for peptide synthesis using N-acylpyrazoles

New system of peptide synthesis was described. The extension of one amino acid unit on the peptide chain was constituted from only 2 reaction steps, the conversion from esters to the corresponding N-acylpyrazoles and the subsequent aminolysis with amino esters. This new system was distinctive from the conventional peptide synthesis, which was consisted of 3 steps of the deprotection, the activation and the condensation. Moreover, the key intermediate N-acylpyrazoles exhibited the excellent properties of high sensitivity and separability for the chiral column on HPLC using the UV detector.