39692-63-2 Usage
General Description
Z-DEHYDRO-ALA-OH is a chemical compound that belongs to the family of dehydroalanine derivatives. It is a modified form of the amino acid alanine, containing a Z-configuration of the dehydroalanine group. Z-DEHYDRO-ALA-OH has been studied for its potential use in peptide and protein engineering, as well as in the development of novel pharmaceuticals and bioactive molecules. Z-DEHYDRO-ALA-OH may also have applications in chemical biology research and the study of protein structure and function. Its unique structure and properties make it a valuable tool for investigating the role of dehydroalanine residues in biological systems and for the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 39692-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,9 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39692-63:
(7*3)+(6*9)+(5*6)+(4*9)+(3*2)+(2*6)+(1*3)=162
162 % 10 = 2
So 39692-63-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO4/c1-8(10(13)14)12-11(15)16-7-9-5-3-2-4-6-9/h2-6H,1,7H2,(H,12,15)(H,13,14)
39692-63-2Relevant articles and documents
Synthesis of nucleo aminooxy acid derivatives
Noel, Olivier,Xie, Juan
, p. 134 - 140 (2013/03/13)
Nucleobase-functionalized peptides have attracted increasing interest because of their well-ordered secondary structures and stability toward enzymatic degradations. We have designed and synthesized nucleo aminooxy acids as novel building blocks for nucle
Synthesis of β-lactam antibiotics by the sulfeno-cycloamination
Ihara,Haga,Yonekura,et al.
, p. 7345 - 7352 (2007/10/02)
A novel efficient beta -lactam synthesis was achieved by two successive processes (sulfeno-cycloamination), addition of phenysulfenyl chloride to alpha , beta -unsaturated amides followed by base treatment. Key synthetic intermediates of monobactams and nocardicin derivatives were obtained via this method. construction of the 1-carbapenam ring system by the sulfenocycloamination is also described.
