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3-Phenyl-[1,2,3]triazole-4-carboxylic acid is a heterocyclic organic compound characterized by its molecular formula C9H7N3O2. It features a triazole ring fused with a phenyl group and a carboxylic acid functionality, making it a valuable building block in organic chemistry. 3-PHENYL-[1,2,3]TRIAZOLE-4-CARBOXYLIC ACID is known for its potential biological activities, such as antifungal, antibacterial, and antitumor properties, and is widely utilized in the synthesis of pharmaceuticals, agrochemicals, and dyes.

15966-72-0

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15966-72-0 Usage

Uses

Used in Pharmaceutical Industry:
3-Phenyl-[1,2,3]triazole-4-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its potential biological activities. It contributes to the development of drugs with antifungal, antibacterial, and antitumor properties, offering therapeutic benefits in treating infections and cancer.
Used in Agrochemical Industry:
In the agrochemical industry, 3-Phenyl-[1,2,3]triazole-4-carboxylic acid serves as a crucial component in the production of pesticides and other agrochemicals. Its incorporation enhances the effectiveness of these products, providing protection against pests and diseases in agriculture.
Used in Dye Industry:
3-Phenyl-[1,2,3]triazole-4-carboxylic acid is used as a building block in the synthesis of dyes, imparting color and stability to various materials. Its unique structure and properties make it suitable for creating dyes with specific characteristics, such as colorfastness and resistance to fading.
Used in Organic Chemistry Research:
As a versatile building block, 3-Phenyl-[1,2,3]triazole-4-carboxylic acid is extensively used in organic chemistry research for the development of new compounds and materials. Its reactivity and functional groups enable the synthesis of a wide range of organic molecules, driving innovation in various fields of research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 15966-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,6 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15966-72:
(7*1)+(6*5)+(5*9)+(4*6)+(3*6)+(2*7)+(1*2)=140
140 % 10 = 0
So 15966-72-0 is a valid CAS Registry Number.

15966-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyltriazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-phenyl-1H-1,2,3-triazole-5-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:15966-72-0 SDS

15966-72-0Relevant academic research and scientific papers

CALPAIN MODULATORS AND THERAPEUTIC USES THEREOF

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Paragraph 1277, (2018/04/17)

Disclosed herein are small molecule calpain modulator compositions, pharmaceutical compositions, the use and preparation thereof.

UNSATURATED CARBONYL-CONTAINING COMPOUNDS. XXVIII. CYCLOADDITION OF ORGANIC AZIDES TO α-ACETYLENIC KETONES AND ACIDS

Vereshchagin, L. I.,Tikhonova, L. G.,Maksikova, A. V.,Serebryakova, E. S.,Proidakov, A. G.,Filippova, T. M.

, p. 641 - 648 (2007/10/02)

The reaction of α-acetylenic ketones and acids with organic azides leads to the formation of 1-alkyl(aryl)-4-acyl(carboxy)-1,2,3-triazoles or to a mixture of the 1,4- and 1,5-disubstituted isomers.The effect of the structure of the initial compound and of the solvent on the direction of cycloaddition was investigated.

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