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1,5-Diphenyl-1H-[1,2,3]triazole-4-carboxylic acid is a chemical compound with the molecular formula C17H12N3O2. It is a derivative of the [1,2,3]triazole ring system, which is a five-membered heterocyclic ring containing three nitrogen atoms. 1, 5-Diphenyl-1H-[1, 2, 3]triazole-4-carboxylic acid features two phenyl groups attached to the 1 and 5 positions of the triazole ring, and a carboxylic acid group at the 4 position. It is known for its potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science, due to its unique structure and properties. The synthesis and functionalization of 1, 5-Diphenyl-1H-[1, 2, 3]triazole-4-carboxylic acid can lead to the development of new molecules with specific biological activities or material properties.

4900-34-9

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4900-34-9 Usage

Class

Triazole carboxylic acids

Structure

Contains a triazole ring with two phenyl groups

Pharmaceutical applications

Used in the synthesis of novel triazole derivatives with potential biological activities

Agricultural applications

Used in the synthesis of novel triazole derivatives with potential biological activities

Anti-tumor potential

Studied for its potential as an anti-tumor agent

Antibacterial potential

Studied for its potential as an antibacterial agent

Antifungal potential

Studied for its potential as an antifungal agent

Corrosion inhibition

Explored for its potential use as a corrosion inhibitor in materials science

Versatility

Wide range of potential applications in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 4900-34-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,0 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4900-34:
(6*4)+(5*9)+(4*0)+(3*0)+(2*3)+(1*4)=79
79 % 10 = 9
So 4900-34-9 is a valid CAS Registry Number.

4900-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-diphenyltriazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1,5-diphenyl-1,2,3-triazole-4-carboxylic acid

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:4900-34-9 SDS

4900-34-9Relevant academic research and scientific papers

Reactions of 2-Benzylidenemalononitrile and 2-Nitro-3-phenylacrylonitrile with Aryl Azides

Nosachev,Shchurova,Tyrkov

, p. 577 - 580 (2011/07/30)

Reactions of 2-benzylidenemalononitrile and 2-nitro-3-phenylacrylonitrile with aryl azides in diethyl ether at room temperature gave mixtures of regioisomeric 1(3)-aryl-5-phenyl-4,5-dihydro-1(3)H-1,2,3- triazole-4,4- dicarbonitriles and 1-aryl-5(4)-phenyl-1H-1,2,3-triazole-5(4)-carbonitriles, respectively. 2-Benzylidenemalononitrile reacted with the same arylazides on heating in boiling chloroform to produce 1-aryl-2- phenylaziridine-2,2- dicarbonitriles. Pleiades Publishing, Ltd., 2011.

Direct synthesis of 1,5-disubstituted-4-magnesio-1,2,3-triazoles, revisited

Krasinski, Antoni,Fokin, Valery V.,Sharpless, K. Barry

, p. 1237 - 1240 (2007/10/03)

After revisiting earlier works reporting the regioselective synthesis of 1,5-disubstituted-1,2,3-triazoles via the addition of bromomagnesium acetylides to azides, much improved yields of the products were obtained for a wide array of azides and alkynes. The intermediates of that reaction can be trapped with different electrophiles to regioselectively form 1,4,5-trisubstituted 1,2,3-triazoles.

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