26607-52-3

Basic information

• Product Name: Cbz-Ala-OH*DCHA
• Synonyms: Cbz-Ala-OH*DCHA
• CAS NO: 26607-52-3
• Molecular Weight: 404.55
• Mol File: 26607-52-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Cbz-Ala-OH*DCHA(CAS DataBase Reference)
• NIST Chemistry Reference: Cbz-Ala-OH*DCHA(26607-52-3)
• EPA Substance Registry System: Cbz-Ala-OH*DCHA(26607-52-3)

Safety Data

• Hazardous Substances Data: 26607-52-3(Hazardous Substances Data)

Upstream product

• 1142-20-7 N-Cbz-Ala 
• 101-83-7 N-cyclohexyl-cyclohexanamine 
• 56-41-7 L-alanin 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 41041-52-5 Z-Ala-Met-OEt 
• 62188-81-2 Z-Ala-Met-OMe 
• 3235-14-1 (S)-2-((S)-2-Benzyloxycarbonylamino-propionylamino)-3-phenyl-propionic acid methyl ester 
• 22610-33-9 (2S,2'S)-N-(N-Benzyloxycarbonylalanyl)proline methyl ester 
• 4864-39-5 N-carbobenzoxy-L-alanyl-L-leucine methyl ester 
• 4864-38-4 (S)-2-((S)-2-Benzyloxycarbonylamino-propionylamino)-3-methyl-butyric acid methyl ester 
• 5673-69-8 N-benzyloxycarbonyl-L-alanyl-L-alanine ethyl ester 
• 2503-32-4 ethyl N-(benzyloxycarbonyl)-L-alanylglycinate 
• 2483-51-4 N-[(benzyloxy)carbonyl]-L-alanyl-L-alanine methyl ester 
• 4840-29-3 Z-L-Ala-Gly-OMe 

Relevant articles and documents

Efficient and practical procedure for the esterification of the free α-carboxylic acid of amino acid residues with β-(trimethylsilyl)ethoxymethyl chloride and triisopropylsilyl chloride

An efficient and practical procedure for the free α-carboxylic acid esterification of amino acid residues with β-(trimethylsilyl)ethoxymethyl chloride and triisopropylsilyl chloride is described. The reaction takes place under mild conditions and the expected protected amino acids are obtained in good to excellent yields. Our method provides a useful alternative for the C-terminal carboxylic acid protection of amino acids and peptides. Moreover, the removal of such protection was also achieved under mild conditions, without affecting either the other protecting groups at the α-amino moiety and side chains or the optical integrity at the α-position of the amino acid residues. Examples of their use in peptide synthesis are also illustrated.