1420537-04-7 Usage
General Description
(R)-tert-butyl 3-(2-aMinoethyl)pyrrolidine-1-carboxylate is a chemical compound with a molecular formula of C11H22N2O2. It is a chiral compound, meaning it has a non-superimposable mirror image, and exists as a single enantiomer. (R)-tert-butyl 3-(2-aMinoethyl)pyrrolidine-1-carboxylate is commonly used as a building block in the synthesis of pharmaceuticals and other organic compounds. Its structure consists of a pyrrolidine ring with a carboxylate group attached to the third carbon atom and an aminoethyl group attached to the second carbon atom. The tert-butyl group is attached to the nitrogen of the pyrrolidine ring, providing steric hindrance and enhancing its stability. (R)-tert-butyl 3-(2-aMinoethyl)pyrrolidine-1-carboxylate is important for its role in chemical synthesis and its potential applications in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 1420537-04-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,0,5,3 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1420537-04:
(9*1)+(8*4)+(7*2)+(6*0)+(5*5)+(4*3)+(3*7)+(2*0)+(1*4)=117
117 % 10 = 7
So 1420537-04-7 is a valid CAS Registry Number.
1420537-04-7Relevant articles and documents
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.
