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1-(3-chlorophenyl)-1H-1,2,3-triazole-4-carboxylic acid is a chemical compound with the molecular formula C9H6ClN3O2. It belongs to the class of triazole carboxylic acids and is structurally composed of a 1,2,3-triazole ring substituted with a 3-chlorophenyl group and a carboxylic acid moiety. 1-(3-chlorophenyl)-1H-1,2,3-triazole-4-carboxylic acid has potential applications in various fields including pharmaceuticals, agrochemicals, and materials science. It may exhibit bioactive and pharmacological properties due to its structural features, and its synthesis and derivatives could be of interest for further research and development in the chemical and pharmaceutical industries.

944901-58-0

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944901-58-0 Usage

Uses

Used in Pharmaceutical Industry:
1-(3-chlorophenyl)-1H-1,2,3-triazole-4-carboxylic acid is used as a pharmaceutical intermediate for the development of new drugs. Its unique structural features allow it to be a potential candidate for the treatment of various diseases and disorders.
Used in Agrochemical Industry:
1-(3-chlorophenyl)-1H-1,2,3-triazole-4-carboxylic acid is used as an agrochemical intermediate for the synthesis of pesticides and other crop protection agents. Its bioactive properties can contribute to the development of effective and environmentally friendly solutions for agriculture.
Used in Materials Science:
1-(3-chlorophenyl)-1H-1,2,3-triazole-4-carboxylic acid is used as a building block in the synthesis of new materials with potential applications in various industries. Its structural features can be utilized to create innovative materials with unique properties and functions.

Check Digit Verification of cas no

The CAS Registry Mumber 944901-58-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,9,0 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 944901-58:
(8*9)+(7*4)+(6*4)+(5*9)+(4*0)+(3*1)+(2*5)+(1*8)=190
190 % 10 = 0
So 944901-58-0 is a valid CAS Registry Number.

944901-58-0SDS

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 1-(3-chlorophenyl)triazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:944901-58-0 SDS

944901-58-0Relevant academic research and scientific papers

One-Pot Synthesis of 1-Monosubstituted 1,2,3-Triazoles from Propargyl Alcohol

Han, Chunmei,Dong, Suping,Zhang, Wensheng,Chen, Zhen

supporting information, p. 673 - 677 (2018/03/10)

A one-pot synthesis of 1-monosubstituted-1,2,3-triazoles from propargyl alcohol and various aryl azides was achieved. This simple method provides concise and efficient access to various 1-monosubstituted 1,2,3-triazole derivatives through a three-step one

Synthesis of 1,2,3-triazole hydrazide derivatives exhibiting anti-phytopathogenic activity

Wang, Xing,Dai, Zhi-Cheng,Chen, Yong-Fei,Cao, Ling-Ling,Yan, Wei,Li, Sheng-Kun,Wang, Jian-Xin,Zhang, Zheng-Guang,Ye, Yong-Hao

, p. 171 - 182 (2016/10/25)

A series of new 1,2,3-triazole derivatives have been prepared and screened for their antifungal activity against phytopathogenic fungi using the mycelium growth inhibition method in?vitro. The results indicated that the 1,2,3-triazole hydrazide scaffold d

Triazole containing novobiocin and biphenyl amides as Hsp90 C-terminal inhibitors

Zhao, Jinbo,Zhao, Huiping,Hall, Jessica A.,Brown, Douglas,Brandes, Eileen,Bazzill, Joseph,Grogan, Patrick T.,Subramanian, Chitra,Vielhauer, George,Cohen, Mark S.,Blagg, Brian S. J.

supporting information, p. 1317 - 1323 (2014/10/15)

Hsp90 C-terminal inhibitors are advantageous for the development of new cancer chemotherapeutics due to their ability to segregate client protein degradation from induction of the prosurvival heat shock response, which is a major detriment associated with

TETRAHYDROISOQUINOLINES CONTAINING SUBSTITUTED AZOLES AS FACTOR XIA INHIBITORS

-

, (2014/10/15)

The present invention provides compounds of Formula (I), or stereoisomers, tautomers, or pharmaceutically acceptable salts thereof, wherein all the variables are as defined herein. These compounds are selective factor XIa inhibitors or dual inhibitors of FXIa and plasma kallikrein. This invention also relates to pharmaceutical compositions comprising these compounds and methods of treating thromboembolic and/or inflammatory disorders using the same.

NOVEL MACROCYCLES AS FACTOR XIA INHIBITORS

-

, (2013/03/26)

The present invention provides compounds of Formula (Ia): or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt thereof, wherein all the variables are as defined herein. These compounds are selective factor XIa inhibitors or dual inhibitors of FXIa and plasma kallikrein. This invention also relates to pharmaceutical compositions comprising these compounds and methods of treating thromboembolic and/or inflammatory disorders using the same.

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