98495-32-0 Usage
Description
3-Pyridinecarboximidic acid, hydrazide is a heterocyclic chemical compound characterized by the presence of a pyridine ring, a carboximidic acid functional group, and a hydrazide moiety. It is known for its potential applications in organic synthesis and pharmaceuticals, as well as its unique structure and chemical properties that make it a valuable compound for research and industrial applications.
Uses
Used in Organic Synthesis:
3-Pyridinecarboximidic acid, hydrazide is used as a building block in the synthesis of a variety of organic compounds, contributing to the development of new chemical entities and materials.
Used in Pharmaceutical Industry:
3-Pyridinecarboximidic acid, hydrazide is used as a potential antimicrobial agent, exhibiting activity against various microorganisms, which makes it a promising candidate for the development of new antibiotics.
Used in Drug Development:
3-Pyridinecarboximidic acid, hydrazide is investigated for its potential as an anti-tuberculosis agent, offering a new avenue for the treatment of tuberculosis and contributing to the fight against drug-resistant strains.
Used in Research Applications:
3-Pyridinecarboximidic acid, hydrazide is utilized in various research applications to explore its chemical properties, reactivity, and potential interactions with other compounds, further expanding its applications in the scientific community.
Check Digit Verification of cas no
The CAS Registry Mumber 98495-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,4,9 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98495-32:
(7*9)+(6*8)+(5*4)+(4*9)+(3*5)+(2*3)+(1*2)=190
190 % 10 = 0
So 98495-32-0 is a valid CAS Registry Number.
98495-32-0Relevant articles and documents
Synthesis and Stability of Boratriazaroles
Zurwerra, Didier,Quetglas, Vincent,Kloer, Daniel P.,Renold, Peter,Pitterna, Thomas
, p. 74 - 77 (2015)
We describe the synthesis and stability analysis of novel boratriazaroles that can be viewed as bioisosteres of imidazoles or pyrazoles. These heterocycles could conveniently be obtained by condensing a boronic acid and amidrazone 1 in various solvents. A detailed stability analysis of selected compounds at different pH values as a function of time led to the identification of steric hindrance around the boron atom as a key element for stabilization. (Chemical Presented).
Synthesis of 2-pyridylpyridines via aza-Diels-Alder reactions between 3-pyridyl-1,2,4-triazines and some vinyl alkanoates
Shintou, Taichi,Ikeuchi, Fumiaki,Kuwabara, Hirokazu,Umihara, Ken,Itoh, Isamu
, p. 836 - 837 (2007/10/03)
New synthetic procedure for 2,ω-bipyridines involving aza-Diels-Alder reaction between 3-(ω-pyridyl)-1,2,4-triazine and vinyl octanoate or decanoate as a dienophile is described. Copyright
