198225-13-7 Usage
Uses
Used in Pharmaceutical Industry:
(S)-1-[2-((S)-sec-Butylamino)-acetyl]-pyrrolidine-2-carboxylic acid benzyl ester is used as a key intermediate in the synthesis of various pharmaceuticals due to its unique structural features and potential for creating biologically active molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-1-[2-((S)-sec-Butylamino)-acetyl]-pyrrolidine-2-carboxylic acid benzyl ester serves as a valuable compound for the development of new drugs. Its structural properties allow for the exploration of its potential in targeting specific biological pathways and creating novel therapeutic agents.
Used in Biochemical Research:
(S)-1-[2-((S)-sec-Butylamino)-acetyl]-pyrrolidine-2-carboxylic acid benzyl ester is also used as a building block in biochemical research for creating new chemical entities. Its complex structure and functional groups make it an interesting candidate for studying interactions with biological systems and potentially discovering new mechanisms of action.
Used in Drug Development:
In the drug development process, (S)-1-[2-((S)-sec-Butylamino)-acetyl]-pyrrolidine-2-carboxylic acid benzyl ester may be employed as a starting material or a component in the synthesis of new drug candidates. Its versatility in organic synthesis and potential for creating biologically active molecules make it a valuable asset in the search for novel therapeutics.
Check Digit Verification of cas no
The CAS Registry Mumber 198225-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,2,2 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 198225-13:
(8*1)+(7*9)+(6*8)+(5*2)+(4*2)+(3*5)+(2*1)+(1*3)=157
157 % 10 = 7
So 198225-13-7 is a valid CAS Registry Number.
198225-13-7Relevant academic research and scientific papers
Glycosylated peptoids as prototypical HIV-1 protease inhibitors
Saha, Uttam K.,Roy, Rene
, p. 7697 - 7700 (2007/10/03)
Using a blockwise approach, N-substituted oligoglycine (NSGs) peptoids bearing N-acetylglucosamine residues in different position of the side chain were efficiently synthesized by a reiterative strategy involving mono N- alkylation and bromoacetylation.
