75415-03-1 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
2-(1H-Pyrazol-3-yl)pyridine is used as a research compound for exploring its potential biological activities and therapeutic properties. It is particularly valuable for its possible applications in the development of new drugs targeting various diseases.
Used in Enzyme Inhibition:
2-(1H-Pyrazol-3-yl)pyridine is used as an enzyme inhibitor, where its structure may interact with specific enzymes to modulate their activity. This application is crucial in the treatment of diseases where enzyme dysregulation plays a significant role.
Used in the Synthesis of Other Organic Compounds:
In the field of medicinal chemistry and pharmaceuticals, 2-(1H-Pyrazol-3-yl)pyridine serves as an intermediate in the synthesis of other organic compounds. Its unique structure allows for the creation of a variety of molecules with potential applications in medicine.
Used in the Treatment of Various Diseases:
Although the specific diseases are not listed in the provided materials, the compound's potential applications in the treatment of various diseases suggest that it may be used as a therapeutic agent, targeting specific biological pathways or mechanisms related to the diseases of interest.
Check Digit Verification of cas no
The CAS Registry Mumber 75415-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,1 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75415-03:
(7*7)+(6*5)+(5*4)+(4*1)+(3*5)+(2*0)+(1*3)=121
121 % 10 = 1
So 75415-03-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3/c1-2-5-9-7(3-1)8-4-6-10-11-8/h1-6H,(H,10,11)
75415-03-1Relevant academic research and scientific papers
Asymmetric Catalysis, 77. - New Optically Active Pyrazole Derivatives for Enantioselective Catalysis
Brunner, Henri,Scheck, Thomas
, p. 701 - 710 (2007/10/02)
Starting from the amines 3-6 and the dipyrazolopyrazinedione 2, the optically active (pyrazolylmethyl)amines 11-14 have been synthesized.Furthermore, the preparation of the (+)-camphor-derived optically active pyrazole 17 is described.Pyrazoles 11-13 and 17 are introduced as chiral building blocks into the 2-(1-pyrazolyl)pyridines 30-33.The optically active compounds 23-25 are formed from 2-pyridine and 2,6-bispyridine, respectively, and (+)-3-(bromomethyl)pinane.The pyrazole derivatives 27-29 contain (+)-(1-phenylethyl)hydrazine as the optically active component.Key Words: Pyrazoles, optically active / Pyridines, 2--, 2,6-bis-, 2-(1-pyrazolyl)-