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3,5-Di(3-pyridinyl)-4H-1,2,4-triazol-4-amine is a chemical compound with the molecular formula C9H8N8. It is a triazol-4-amine derivative featuring two 3-pyridinyl substituents. 3,5-DI(3-PYRIDINYL)-4H-1,2,4-TRIAZOL-4-AMINE is recognized for its versatile reactivity and application in organic chemistry, making it a valuable building block in the synthesis of pharmaceuticals and agrochemicals. Its structural characteristics and functional groups contribute to its role as an important intermediate in the production of biologically active compounds and as a candidate for drug research. Furthermore, it has been investigated for potential biological activities, such as antimicrobial and anti-cancer properties.

38629-66-2

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38629-66-2 Usage

Uses

Used in Pharmaceutical Industry:
3,5-Di(3-pyridinyl)-4H-1,2,4-triazol-4-amine is used as a building block for the synthesis of various pharmaceuticals due to its versatile reactivity and structural characteristics. It aids in the development of biologically active compounds and serves as an intermediate in the production of potential drug candidates.
Used in Agrochemical Industry:
In the agrochemical sector, 3,5-Di(3-pyridinyl)-4H-1,2,4-triazol-4-amine is utilized as a key component in the synthesis of agrochemicals, contributing to the creation of effective and novel products for agricultural applications.
Used in Organic Chemistry Research:
3,5-Di(3-pyridinyl)-4H-1,2,4-triazol-4-amine is employed as a research compound in organic chemistry, where its unique properties are explored for the development of new chemical reactions and the synthesis of complex organic molecules.
Used in Antimicrobial Applications:
3,5-DI(3-PYRIDINYL)-4H-1,2,4-TRIAZOL-4-AMINE is studied for its potential antimicrobial properties, making it a candidate for use in applications that require the inhibition of microbial growth, such as in medical and industrial settings.
Used in Anti-cancer Research:
3,5-Di(3-pyridinyl)-4H-1,2,4-triazol-4-amine is investigated for its potential anti-cancer properties, with the aim of identifying its role in the development of new therapeutic agents for cancer treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 38629-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,2 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38629-66:
(7*3)+(6*8)+(5*6)+(4*2)+(3*9)+(2*6)+(1*6)=152
152 % 10 = 2
So 38629-66-2 is a valid CAS Registry Number.

38629-66-2Downstream Products

38629-66-2Relevant academic research and scientific papers

Synthesis, crystal structure, and luminescent properties of a novel cadmium coordination polymer

He, Yong,Chu, Wen-Juan,Duan, Lu-Meng,Fan, Yao-Ting,Hou, Hong-Wei

, (2012)

A novel cadmium metal-organic coordination polymer, namely Cd(atda)(3-abpt)(H2O)·2H2O (H2 atda = (4-amino-1,2,4-triazole- 3,5-diyldithio) diacetic acid, 3-abpt = 4-amino-3,5-bis(3-pyridyl)- 1,2,4-triazole)), has been obtai

A facile and solvent-free synthesis of 3,5 -disubstituted-4-amino-1,2,4-triazoles by reactions of aromatic nitriles with hydrazine

Ikemi, Yukio,Hayashi, Naoto,Kakehi, Akikazu,Matsumoto, Kiyoshi

, p. 439 - 442 (2007/10/03)

A variety of 3, 5-disubstituted-4-amino-1,2,4-triazoles were prepared by reactions of aromatic nitriles with hydrazine monohydrate. The structure of 3,5-diphenyl-4-amino-1,2,4-triazole was established by an X-ray analysis.

A simple one step synthesis of new 3,5-disubstituted-4-amino-1,2,4- triazoles

Bentiss,Lagrenee,Traisnel,Mernari,Elattari

, p. 149 - 152 (2007/10/03)

A number of symmetrically 3,5-disubstituted 4-amino-1,2,4-triazoles have been prepared by the reaction of aromatic nitriles with hydrazine dihydrochloride or sulfate with an excess of hydrazine hydrate in ethylene or diethylene glycol under a nitrogen atm

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