1198-83-0 Usage
Uses
Used in Medicinal Chemistry:
2-methylsulfanyl-7H-purin-6-amine is used as a research compound for exploring its potential biological activities and pharmacological properties. Its unique structure allows it to be a valuable tool in the development of new drugs and therapeutic agents.
Used in Drug Development:
In the pharmaceutical industry, 2-methylsulfanyl-7H-purin-6-amine is used as a lead compound for the design and synthesis of novel therapeutic agents. Its potential applications may include the treatment of various diseases and conditions, given its interaction with biological targets and systems.
Used in Biochemical Research:
2-methylsulfanyl-7H-purin-6-amine serves as a subject of study in biochemical research to understand its interactions with enzymes, receptors, and other biomolecules. This knowledge can contribute to the advancement of our understanding of biological processes and the development of targeted therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 1198-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1198-83:
(6*1)+(5*1)+(4*9)+(3*8)+(2*8)+(1*3)=90
90 % 10 = 0
So 1198-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N5S/c1-12-6-10-4(7)3-5(11-6)9-2-8-3/h2-3H,1H3,(H2,7,8,9,10,11)
1198-83-0Relevant articles and documents
BF3·SMe2 for Thiomethylation, Nitro Reduction and Tandem Reduction/SMe Insertion of Nitrogen Heterocycles
S?derstr?m, Marcus,Zamaratski, Edouard,Odell, Luke R.
, p. 5402 - 5408 (2019/06/27)
Herein, a general, solvent-free and straightforward thiomethylation of electron deficient heterocycles using BF3·SMe2 as a dual thiomethyl source and Lewis acidic activator is presented. A range of heterocycles including pyrimidine, pyrazine, pyridazine, thiazole and purine derivatives were successfully substituted using this method. An unexpected reductive property of BF3·SMe2 towards nitropyridines was also discovered including an intriguing tandem reduction/SMe insertion process in certain substrates. Notable features of the present work include its convenience and use of a non-malodorous reagent while the discovery of novel chemical transformations using BF3·SMe2 provides fundamental new insights into the reactivity of this commonly employed reagent.