3401-33-0 Usage
Uses
Used in Pharmaceutical Industry:
Boc-S-benzyl-L-cysteine N-hydroxysuccinimide ester is used as a synthetic intermediate for the development of peptide-based drugs. Its ability to form stable amide bonds with amino groups enables the creation of novel therapeutic agents with enhanced stability and bioactivity.
Used in Biotechnology Industry:
In the biotechnology field, Boc-S-benzyl-L-cysteine N-hydroxysuccinimide ester is used as a protein modification reagent. It allows for the targeted attachment of various functional groups to proteins, facilitating the exploration of protein function and the development of new biotechnological applications.
Used in Drug Development:
Boc-S-benzyl-L-cysteine N-hydroxysuccinimide ester is employed as a key component in the synthesis of bioactive peptides and proteins. Its role in forming stable amide bonds is crucial for the development of drugs with improved pharmacokinetic properties and therapeutic efficacy.
Used in Proteomics Research:
Boc-S-benzyl-L-cysteine N-hydroxysuccinimide ester is utilized as a tool for protein modification in proteomics studies. Its reactivity with cysteine residues allows for the specific labeling and detection of proteins, contributing to a deeper understanding of protein function and interactions within complex biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 3401-33-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3401-33:
(6*3)+(5*4)+(4*0)+(3*1)+(2*3)+(1*3)=50
50 % 10 = 0
So 3401-33-0 is a valid CAS Registry Number.
3401-33-0Relevant academic research and scientific papers
Novel Preparation of N-Protected Amino Acid Active Esters Using 1,2,2,2-Tetrachloroethyl Carbonates
Jaoudai, Mahmoud,Martinez, Jean,Castro, Bertrand
, p. 2364 - 2367 (2007/10/02)
1,2,2,2-Tetrachloroethyl chloroformate reacts with substituted phenols or N-hydroxy imides to yield crystalline and stable mixed aryl or oximido tetrachloroethyl carbonates.When allowed to react with an N-protected amino acid derivative, these compounds proved to be efficient for the syntheses of the corresponding active esters.A series of active esters including p-nitrophenol, trichlorophenol, pentafluorophenol, and N-hydroxysuccinimide derivatives were prepared by this new procedure.
