54784-68-8 Usage
Description
S-[(Acetylamino)methyl]-N-[(benzyloxy)carbonyl]-L-cysteine is a derivative of the amino acid cysteine, featuring an acetylamino group and a benzyloxy carbonyl group. S-[(Acetylamino)methyl]-N-[(benzyloxy)carbonyl]-L-cysteine is integral to numerous biochemical processes and is extensively utilized in the synthesis of peptides and proteins in biochemistry and pharmaceutical research.
Uses
Used in Biochemistry and Pharmaceutical Research:
S-[(Acetylamino)methyl]-N-[(benzyloxy)carbonyl]-L-cysteine is used as a building block for the synthesis of peptides and proteins. Its acetylamino group is crucial for modifying the structure and function of proteins, enhancing their stability and activity.
Used as a Protective Group:
In the pharmaceutical industry, the benzyloxy carbonyl group in S-[(Acetylamino)methyl]-N-[(benzyloxy)carbonyl]-L-cysteine serves as a protective group for thiol-containing molecules, safeguarding them from unwanted reactions during the synthesis process.
Used in Drug Production:
S-[(Acetylamino)methyl]-N-[(benzyloxy)carbonyl]-L-cysteine is employed in the production of pharmaceutical drugs, where its unique properties contribute to the development of novel therapeutic agents.
Used in Enzyme Catalysis and Protein Folding Studies:
S-[(Acetylamino)methyl]-N-[(benzyloxy)carbonyl]-L-cysteine is also utilized in the study of enzyme catalysis and protein folding, providing insights into the mechanisms of these biological processes and aiding in the design of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 54784-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,8 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54784-68:
(7*5)+(6*4)+(5*7)+(4*8)+(3*4)+(2*6)+(1*8)=158
158 % 10 = 8
So 54784-68-8 is a valid CAS Registry Number.
54784-68-8Relevant articles and documents
A general and versatile route to "zinc finger" templates
Ranganathan, Subramania,Jayaraman, Narayanaswamy
, p. 6681 - 6682 (2007/10/02)
The basic zinc finger template is formed in a single step from PNHCys[ S- CH,2NHAc ] HisOMe and zinc chloride by a tandem complexation deprotection sequence.
