60637-33-4 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
2-Chloro-pyrazolo[1,5-a]pyridine is utilized as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with potential therapeutic and pesticidal properties, contributing to the advancement of these industries.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-Chloro-pyrazolo[1,5-a]pyridine serves as a valuable reagent for the preparation of novel organic compounds with potential biological activity. Its incorporation into drug discovery pipelines facilitates the exploration of new chemical entities that may address unmet medical needs.
Used in Chemical Research and Development:
2-Chloro-pyrazolo[1,5-a]pyridine is employed as a research reagent for the synthesis and study of other organic compounds. Its unique structural features make it an attractive candidate for investigating new chemical reactions and exploring the properties of newly synthesized compounds, thereby expanding the scope of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 60637-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,3 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60637-33:
(7*6)+(6*0)+(5*6)+(4*3)+(3*7)+(2*3)+(1*3)=114
114 % 10 = 4
So 60637-33-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H5ClN2/c8-7-5-6-3-1-2-4-10(6)9-7/h1-5H
60637-33-4Relevant articles and documents
Synthesis of 2-Arylpyrazolo[1,5- a ]pyridines by Suzuki-Miyaura Cross-Coupling Reaction
Umei, Kentaro,Nishigaya, Yosuke,Kamiya, Megumi,Kohno, Yasushi,Seto, Shigeki
, p. 3221 - 3230 (2015/10/19)
Convenient access to a variety of 2-arylated pyrazolo[1,5-a]pyridine via pyrazolo[1,5-a]pyridine-2-yl triflate using the Suzuki-MiyauraA AA cross-coupling reaction is described. Fifteen 2-arylpyrazolo[1,5-a]pyridine derivatives were synthesized in 52-95% yields.
PYRAZOLOPYRIDYL COMPOUNDS AS ALDOSTERONE SYNTHASE INHIBITORS
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Page/Page column 54; 55, (2013/04/10)
This invention relates to pyrazolopyridyl compounds of the structural formula: [Formula should be inserted here] or their pharmaceutically acceptable salts, wherein the variable are defined herein. The inventive compounds selectively inhibit aldosterone s