274692-08-9 Usage
Uses
Used in Organic Synthesis:
(S)-tert-butyl 3-(2-aminoethyl)pyrrolidine-1-carboxylate is used as a chiral building block for the preparation of various biologically active molecules. Its presence in organic synthesis is crucial for the creation of complex organic compounds that require specific stereochemistry.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-tert-butyl 3-(2-aminoethyl)pyrrolidine-1-carboxylate is utilized as a key intermediate for the synthesis of pharmaceuticals. Its chiral nature is particularly valuable for the production of enantiomerically pure compounds, which is essential for the development of many drugs and agrochemicals to ensure efficacy and safety.
Used in the Production of Enantiomerically Pure Compounds:
(S)-tert-butyl 3-(2-aminoethyl)pyrrolidine-1-carboxylate is employed as a precursor in the synthesis of enantiomerically pure compounds. The importance of enantiomeric purity in pharmaceuticals and agrochemicals cannot be overstated, as it directly impacts the effectiveness and potential side effects of these compounds.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (S)-tert-butyl 3-(2-aminoethyl)pyrrolidine-1-carboxylate is used as a critical component in the development of new drugs. Its role in creating biologically active molecules with specific stereochemistry is vital for the advancement of medicines with targeted therapeutic effects and minimized side effects.
Used in Agrochemical Development:
Similarly, in agrochemical development, (S)-tert-butyl 3-(2-aminoethyl)pyrrolidine-1-carboxylate is applied as a building block for the synthesis of enantiomerically pure agrochemicals. This ensures that the active ingredients in these products are effective against pests and diseases while minimizing potential environmental and health impacts.
Check Digit Verification of cas no
The CAS Registry Mumber 274692-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,4,6,9 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 274692-08:
(8*2)+(7*7)+(6*4)+(5*6)+(4*9)+(3*2)+(2*0)+(1*8)=169
169 % 10 = 9
So 274692-08-9 is a valid CAS Registry Number.
274692-08-9Relevant academic research and scientific papers
STING AGONISTS AND USES THEREOF
-
, (2020/07/14)
The present invention provides compounds, compositions thereof, and methods of using the same for the modulation of STING, and the treatment of STING-mediated disorders.
Synthesis and antibacterial activity of novel 1 β-methyl carbapenems with cycloalkylamine moiety at the C-2 position
Kawamoto, Isao,Shimoji, Yasuo,Kanno, Osamu,Endo, Rokuro,Miyauchi, Masau,Kojima, Katsuhiko,Ishikawa, Katsuya,Morimoto, Munetsugu,Ohya, Satoshi
, p. 1080 - 1092 (2007/10/03)
Novel 1β-methyl carbapenems with a cycloalkylamine moiety as a side chain were synthesized and their structure-activity relationships were studied. These carbapenems showed potent antibacterial activities against a wide range of range of Gram-positive and Gram-negative bacteria, and moderate urinary recovery when administered intraperitoneally in mice.
