274692-07-8 Usage
General Description
"(R)-3-CYANOMETHYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER" is a type of chemical compound often utilized in the field of synthetic chemistry. Pyrrolidines, the base structure of this compound, are five-membered rings that contain nitrogen, and are common pharmacophores, which are features responsible for a drug's activity. The cyanomethyl functional group, the "R" designation at the beginning, and the tert-butyl ester functional group suggest that this compound is a specific isomer, and it has various potential uses in pharmaceutical applications or chemical reactions. The exact properties and uses of the compound are highly dependent on context and can vary widely based on how it's utilized in a given chemical reaction.
Check Digit Verification of cas no
The CAS Registry Mumber 274692-07-8 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 274692-07:
(8*2)+(7*7)+(6*4)+(5*6)+(4*9)+(3*2)+(2*0)+(1*7)=168
168 % 10 = 8
So 274692-07-8 is a valid CAS Registry Number.
274692-07-8Relevant articles and documents
FUMAGILLOL HETEROCYCLIC COMPOUNDS AND METHODS OF MAKING AND USING SAME
-
, (2017/03/08)
Disclosed herein, in part, are fumagillol compounds and methods of use in treating medical disorders, such as obesity. Pharmaceutical compositions and methods of making fumagillol compounds are provided. The compounds are contemplated to have activity against methionyl aminopeptidase 2.
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.
