6958-73-2 Usage
General Description
5-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene is a chemical compound with a unique molecular structure. It is classified as a bicyclic compound with a sulfur and methyl group attached to the central ring. 5-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene is part of the triazabicyclo nonane family, which is known for its diverse range of applications in organic chemistry and medicinal chemistry. The presence of the sulfur and methyl group provides distinct chemical properties that can be utilized in various chemical reactions and synthesis processes. Its unique structure and properties make it an interesting compound for further research and potential application in pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 6958-73-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6958-73:
(6*6)+(5*9)+(4*5)+(3*8)+(2*7)+(1*3)=142
142 % 10 = 2
So 6958-73-2 is a valid CAS Registry Number.
InChI:InChI=1/C21H18BrN3O/c1-3-26-20-9-8-14(22)10-17(20)16-11-19(25-21(24)18(16)12-23)15-7-5-4-6-13(15)2/h4-11H,3H2,1-2H3,(H2,24,25)
6958-73-2Relevant articles and documents
6-Oxo and 6-thio purine analogs as antimycobacterial agents
Pathak, Ashish K.,Pathak, Vibha,Seitz, Lainne E.,Suling, William J.,Reynolds, Robert C.
, p. 1685 - 1695 (2013/05/09)
6-Oxo and 6-thio analogs of purine were prepared based on the initial activity screening of a small, diverse purine library against Mycobacterium tuberculosis (Mtb). Certain 6-oxo and 6-thio-substituted purine analogs described herein showed moderate to good inhibitory activity. N 9-substitution apparently enhances the anti-mycobacterial activity in the purine series described herein. Several 2-amino and 2-chloro purine analogs were also synthesized that showed moderate inhibitory activity against Mtb.
