6958-73-2 Usage
Uses
Used in Organic Chemistry:
5-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene is used as a building block for the synthesis of various organic compounds due to its unique structure and reactivity. The presence of the sulfur and methyl group allows for a wide range of chemical transformations, making it a valuable component in the development of new organic molecules.
Used in Medicinal Chemistry:
5-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene is used as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structure and properties can be exploited to design and develop novel drugs with potential therapeutic applications. 5-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene's ability to participate in various chemical reactions makes it a promising candidate for the creation of new medicinal agents.
Used in Agrochemicals:
5-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene is used as a starting material for the development of agrochemicals, such as pesticides and herbicides. Its unique chemical properties can be harnessed to create effective and environmentally friendly solutions for agricultural applications.
Used in Materials Science:
5-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene is used as a component in the development of advanced materials with specific properties. Its unique structure and reactivity can contribute to the creation of materials with improved performance in various industries, such as electronics, energy, and nanotechnology.
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 academic research and scientific papers
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.
