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1,4-Diphenyl-5-amino-1,2,3-triazole, also known as diphenylaminotriazole, is a heterocyclic aromatic compound with the molecular formula C14H11N5. It features a triazole ring and two phenyl groups, making it a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and organic dyes.

29704-63-0

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29704-63-0 Usage

Uses

Used in Pharmaceutical Industry:
1,4-Diphenyl-5-amino-1,2,3-triazole is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 1,4-Diphenyl-5-amino-1,2,3-triazole serves as an intermediate in the production of agrochemicals, aiding in the creation of compounds that protect crops and enhance agricultural productivity.
Used in Organic Dyes:
1,4-Diphenyl-5-amino-1,2,3-triazole is utilized as an intermediate in the synthesis of organic dyes, which are essential for coloring fabrics, plastics, and other materials.
Used in Plastics Industry:
As a stabilizer in the plastics industry, 1,4-Diphenyl-5-amino-1,2,3-triazole improves the resistance of polymers to degradation caused by heat, light, and oxidation, thereby extending the lifespan and performance of plastic products.
Used in Electronics and Optoelectronics:
1,4-Diphenyl-5-amino-1,2,3-triazole has potential applications in the development of new materials for electronics and optoelectronics, where its unique properties can be harnessed to create innovative devices and components.

Check Digit Verification of cas no

The CAS Registry Mumber 29704-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,0 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29704-63:
(7*2)+(6*9)+(5*7)+(4*0)+(3*4)+(2*6)+(1*3)=130
130 % 10 = 0
So 29704-63-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N4/c15-14-13(11-7-3-1-4-8-11)16-17-18(14)12-9-5-2-6-10-12/h1-10H,15H2

29704-63-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-diphenyltriazol-4-amine

1.2 Other means of identification

Product number -
Other names 1,4-Diphenyl-5-amino-1,2,3-triazol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:29704-63-0 SDS

29704-63-0Relevant academic research and scientific papers

Designing a new basic ionic liquid [DHIM][OH] as a task specific bifunctional catalyst for facile microwave assisted metal free synthesis of 5-amino-1,2,3-triazoles

Dutta, Bidyutjyoti,Garg, Anirban,Kulshrestha, Akshay,Kumar, Arvind,Phukan, Parmita,Sarma, Diganta

supporting information, p. 12792 - 12797 (2021/08/04)

A green protocol for the synthesis of a series of 5-amino-1,2,3-triazoles from benzyl cyanide and phenyl azide derivatives catalyzed by the novel bifunctional ionic liquid [DHIM][OH] under microwave irradiation has been developed. The bifunctional ionic l

One-Pot Synthesis of 5-Amino-1,2,3-triazole Derivatives via Dipolar Azide?Nitrile Cycloaddition and Dimroth Rearrangement under Solvent-Free Conditions

Gribanov, Pavel S.,Atoian, Edita M.,Philippova, Anna N.,Topchiy, Maxim A.,Asachenko, Andrey F.,Osipov, Sergey N.

supporting information, p. 1378 - 1384 (2021/02/26)

An efficient one-pot methodology for the preparation of 5-amino-1,2,3-triazole derivatives based on the combination of dipolar azide?nitrile cycloaddition with Dimroth rearrangement under solvent-free conditions has been developed.

Azide-acetonitrile "click" reaction triggered by Cs2CO3: The atom-economic, high-yielding synthesis of 5-amino-1,2,3-triazoles

Krishna, Patoju M.,Ramachary, Dhevalapally B.,Peesapati, Sruthi

, p. 62062 - 62066 (2015/08/03)

Medicinally important 5-amino-1,2,3-triazoles were synthesized using a novel Cs2CO3-catalyzed azide-acetonitrile[3 + 2]-cycloaddition. Aryl azides and aryl acetonitriles were employed in this transformation resulting in excellent yie

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