132243-26-6 Usage
Class
Beta-lactams
Uses
Intermediate in the synthesis of pharmaceuticals, particularly antibiotics such as penicillin and cephalosporin
Properties
Potential antibacterial and antifungal agent
Application
Studied for potential use in medicinal chemistry for development of new drugs
Check Digit Verification of cas no
The CAS Registry Mumber 132243-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,4 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132243-26:
(8*1)+(7*3)+(6*2)+(5*2)+(4*4)+(3*3)+(2*2)+(1*6)=86
86 % 10 = 6
So 132243-26-6 is a valid CAS Registry Number.
132243-26-6Relevant articles and documents
Synthesis of carbocyclic nucleosides from 2-azabicyclo[2.2.1]hept-5-en-3-ones: Sodium borohydride-mediated carbon-nitrogen bond cleavage of five- and six-membered lactams
Katagiri,Muto,Nomura,Higashikawa,Kaneko
, p. 1112 - 1122 (2007/10/02)
Various carbocyclic ribofuranosyl nucleosides were stereoselectively synthesized through a small number of steps from 2-azabicyclo[2.2.1]hept-5-en-3-ones by the use of sodium borohydride-mediated C-N bond cleavage as a key step. Ready availability of a no
