2488-18-8 Usage
Uses
Used in Pharmaceutical Industry:
BOC-MET-ONP is used as a building block for the synthesis of peptide-based drugs, contributing to the development of novel therapeutic agents. Its protective and chromophoric properties ensure efficient and accurate peptide synthesis, enhancing drug discovery and production processes.
Used in Research and Development:
BOC-MET-ONP is employed as a key component in the synthesis of research tools, enabling scientists to create and study peptides for various biological and medical applications. Its protective and chromophoric features facilitate precise and reliable peptide synthesis, supporting innovative research in the field.
Used in Biochemical Probes Production:
BOC-MET-ONP is utilized as a fundamental building block in the creation of biochemical probes, which are essential for investigating biological processes and interactions at the molecular level. Its protective and chromophoric properties ensure the accurate synthesis of these probes, advancing our understanding of complex biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 2488-18-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,8 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2488-18:
(6*2)+(5*4)+(4*8)+(3*8)+(2*1)+(1*8)=98
98 % 10 = 8
So 2488-18-8 is a valid CAS Registry Number.
2488-18-8Relevant academic research and scientific papers
Kinetic Studies in Peptide Chemistry. Coupling, Racemization, and Evaluation of Methods Useful for Shortening Coupling Time
Kovacs, J.,Holleran, E. M.,Hui, K. Y.
, p. 1060 - 1065 (2007/10/02)
Kinetic studies were carried out on N-protected methionine and glycylmethionine active esters to determine the racemization rate constants with triethylamine and the coupling rate constants with valine methyl ester.In contrast to cysteine dipeptide active esters, which racemize through an enolization mechanism, the methionine dipeptide active esters racemize through the usual 5(4H)-oxazolone route.The role of sulfur in the side chain is discussed.The time required for coupling a given percentage (e.g., 99 percent) of the amine component can be significantly reduced by using an excess of the active ester.This method is evaluated quantitatively for second-order kinetics.
