147091-71-2 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-METHYL 2-(TERT-BUTOXYCARBONYLAMINO)-3-CYANOPROPANOATE is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its role in creating complex molecular structures is crucial, as it allows for the development of new and innovative medications.
Used in Organic Compound Synthesis:
In the field of organic chemistry, (S)-METHYL 2-(TERT-BUTOXYCARBONYLAMINO)-3-CYANOPROPANOATE is utilized as an intermediate for the synthesis of a wide range of organic compounds. Its versatility in forming different chemical structures makes it a valuable component in this industry.
Used in Peptide Synthesis:
(S)-METHYL 2-(TERT-BUTOXYCARBONYLAMINO)-3-CYANOPROPANOATE is also employed in the synthesis of peptides. The Boc group present in its structure acts as a protective group for the amino group, facilitating selective reactions and allowing for the formation of specific peptide sequences. This application is particularly important in the development of peptide-based drugs and therapeutics.
Check Digit Verification of cas no
The CAS Registry Mumber 147091-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,0,9 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 147091-71:
(8*1)+(7*4)+(6*7)+(5*0)+(4*9)+(3*1)+(2*7)+(1*1)=132
132 % 10 = 2
So 147091-71-2 is a valid CAS Registry Number.
147091-71-2Relevant academic research and scientific papers
Xue, Chu-Biao,He, Xiaohua,Roderick, John,DeGrado, William F.,Decicco, Carl,Copeland, Robert A.
, p. 379 - 384 (1996)
A series of amino-carboxylate inhibitors of matrix metalloproteinases containing different P1 modifications have been synthesized. It was discovered that a toluenesulfonamide-type substituent at the P1 position considerably enhances the binding affinity of inhibitors for stromelysin. Replacements of the P2'-P3' residues with nonpeptide components result in loss of inhibitory activity.
