25433-36-7 Usage
Description
5-Methyl-3-(pyridin-2-yl)-1H-1,2,4-triazole is a heterocyclic chemical compound with the molecular formula C8H8N4. It belongs to the triazole class of compounds, which are known for their diverse applications in various fields. This molecule features both nitrogen and carbon atoms in its structure, with a pyridine and triazole moiety, making it a promising candidate for the development of new drugs or agrochemicals. Its unique structure and properties have attracted interest in the fields of organic chemistry and chemical biology for further research and development.
Uses
Used in Pharmaceutical Industry:
5-Methyl-3-(pyridin-2-yl)-1H-1,2,4-triazole is used as a potential candidate for the development of new drugs due to its unique structure and properties. The presence of the pyridine and triazole moieties in the molecule allows for the exploration of its potential therapeutic applications, such as antimicrobial, antifungal, or antiviral agents.
Used in Agrochemical Industry:
In the agrochemical industry, 5-Methyl-3-(pyridin-2-yl)-1H-1,2,4-triazole is used as a potential candidate for the development of new agrochemicals. Its unique structure and properties make it a promising candidate for the creation of novel pesticides, herbicides, or fungicides, which can help address the challenges faced in agriculture, such as pest resistance and crop protection.
Used in Materials Science:
5-Methyl-3-(pyridin-2-yl)-1H-1,2,4-triazole is also used in materials science for the development of new materials with specific properties. The triazole moiety in the molecule can be utilized to create materials with unique characteristics, such as high thermal stability, flame retardancy, or specific optical properties, which can be applied in various industries, including electronics, aerospace, and automotive.
Used in Organic Chemistry Research:
5-Methyl-3-(pyridin-2-yl)-1H-1,2,4-triazole serves as an interesting target for researchers in the field of organic chemistry. Its unique structure and properties provide opportunities for the exploration of new synthetic routes, reaction mechanisms, and the development of novel chemical transformations. This can lead to the discovery of new compounds with potential applications in various fields.
Used in Chemical Biology Research:
In chemical biology, 5-Methyl-3-(pyridin-2-yl)-1H-1,2,4-triazole is used for the investigation of its interactions with biological systems. Its unique structure allows researchers to study its binding properties, potential biological activities, and its role in modulating biological processes. This can contribute to the understanding of molecular mechanisms and the development of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 25433-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,3 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25433-36:
(7*2)+(6*5)+(5*4)+(4*3)+(3*3)+(2*3)+(1*6)=97
97 % 10 = 7
So 25433-36-7 is a valid CAS Registry Number.
25433-36-7Relevant articles and documents
Influence of the nature of the substituent in 3-(2-pyridyl)-1,2,4-triazole for complexation with Pd2+
Zakharchenko, Borys V.,Khomenko, Dmytro M.,Doroshchuk, Roman O.,Severynovska, Olga V.,Raspertova, Ilona V.,Starova, Victoria S.,Lampeka, Rostyslav D.
, p. 2003 - 2009 (2017/10/05)
The structure of four new palladium complexes [Pd(HL 2 )Cl 2 and Pd(L 1-3 ) 2 ] with 3-(2-pyridyl)-5-R-1,2,4-triazoles (R=H, CH3, Ph respectively HL 1, HL 2, HL 3 ) wa
Luminescence comparison of iridium(III) complexes containing symmetric vs. asymmetric quinolinate ligands
Park, Hye Rim,Ha, Yunkyoung
scheme or table, p. 67 - 74 (2011/11/29)
We have focused our research on development of the iridium complexes, especially with respect to blue and red emission for OLED. Previously, we prepared bis-[2,3-bis(4-fluorophenyl)quinoxalinato]iridium(acetylacetonate) [Ir(2,3-dpqx-F2)2/
SMALL MOLECULE MODULATORS OF CELL ADHESION
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Page/Page column 41, (2009/12/05)
Compounds, particularly compounds having activity as modulators of cadherin-mediated cell adhesion having the following structure: or a pharmaceutically acceptable salt, stereoisomer or prodrug thereof, wherein R1, R2, R3,