87789-35-3 Usage
Description
5,7-Dichloro-2-(methylthio)thiazolo[4,5-d]pyrimidine is a heterocyclic chemical compound with the molecular formula C7H4Cl2N2S2. It features a thiazole ring fused to a pyrimidine ring, with two chlorine atoms and a methylthio group attached to it. This unique structure and its potential properties make it an intriguing compound for research and development in various fields.
Uses
Used in Pharmaceutical Industry:
5,7-Dichloro-2-(methylthio)thiazolo[4,5-d]pyrimidine is used as a potential anti-cancer and anti-inflammatory agent due to its unique structure and properties. It is being studied for its potential to contribute to the development of new drugs that can address these medical conditions more effectively.
Used in Research and Development:
5,7-Dichloro-2-(methylthio)thiazolo[4,5-d]pyrimidine is also used as a target for further research and development in the pharmaceutical industry. Its distinctive molecular structure suggests that it may hold promise for the creation of innovative therapeutic agents.
While the provided materials do not explicitly mention applications in agriculture or material science, the potential for such uses is suggested due to the compound's unique structure and properties. Further research would be required to explore these possibilities.
Check Digit Verification of cas no
The CAS Registry Mumber 87789-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,8 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87789-35:
(7*8)+(6*7)+(5*7)+(4*8)+(3*9)+(2*3)+(1*5)=203
203 % 10 = 3
So 87789-35-3 is a valid CAS Registry Number.
87789-35-3Relevant articles and documents
THIAZOLOPYRIMIDINE PI3K INHIBITOR COMPOUNDS AND METHODS OF USE
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Page/Page column 94-95, (2009/05/29)
Compounds of Formulas (Ia and Ib), and including stereoisomers, geometric isomers, tautomers, solvates, metabolites and pharmaceutically acceptable salts thereof, are useful for inhibiting lipid kinases including PI3K, and for treating disorders such as cancer mediated by lipid kinases. Methods of using compounds of formula Ia and Ib for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed