109202-21-3 Usage
Uses
Used in Pharmaceutical Industry:
5-chloro-2-methylthiazolo[5,4-b]pyridine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 5-chloro-2-methylthiazolo[5,4-b]pyridine serves as an essential intermediate for the synthesis of novel pesticides. Its chemical properties allow for the creation of effective pest control agents.
Used in Organic Synthesis:
5-chloro-2-methylthiazolo[5,4-b]pyridine is utilized as a versatile building block in organic synthesis, enabling the production of a wide range of organic compounds with diverse applications.
Used in Drug Development:
Due to its potential biological activity, 5-chloro-2-methylthiazolo[5,4-b]pyridine is studied for its possible use in the treatment of various diseases. Its unique structure may offer new avenues for drug discovery and development.
Used in Pesticide Development:
5-chloro-2-methylthiazolo[5,4-b]pyridine's potential applications in the development of new pesticides make it a valuable compound in the agrochemical industry, where it can contribute to the creation of innovative and effective pest control solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 109202-21-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,2,0 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 109202-21:
(8*1)+(7*0)+(6*9)+(5*2)+(4*0)+(3*2)+(2*2)+(1*1)=83
83 % 10 = 3
So 109202-21-3 is a valid CAS Registry Number.
109202-21-3Relevant articles and documents
Nouvelle methode de synthese de thiazolopyridines
Couture, Axel,Grandclaudon, Pierre,Huguerre, Eric
, p. 1765 - 1770 (2007/10/02)
It has been established that the direct condensation between aromatic and aliphatic thioesters and the variously generated anion of aminochloropyridines represents the best method for the synthesis of thiazolopyridines.The transient thioamides, sometimes isolated, can be easily converted chemically or photochemically into the desired fused heterocycles.