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33469-14-6

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33469-14-6 Usage

Description

1H-Imidazole, 2-(3-chlorophenyl)-5-(trifluoroMethyl) is a chemical compound with the molecular formula C10H7ClF3N3. It is a derivative of imidazole, a five-membered heterocyclic ring containing two nitrogen atoms. 1H-IMidazole, 2-(3-chlorophenyl)-5-(trifluoroMethyl) is characterized by a trifluoromethyl group attached to the fifth carbon atom and a chlorophenyl group attached to the second carbon atom of the imidazole ring. Due to the presence of the imidazole ring and the substituted phenyl and trifluoromethyl groups, it may exhibit various biological activities, making it an interesting target for further research and investigation in the field of medicinal chemistry.

Uses

Used in Pharmaceutical Development:
1H-Imidazole, 2-(3-chlorophenyl)-5-(trifluoroMethyl) is used as a potential candidate in pharmaceutical development for its possible biological activities. The presence of the imidazole ring and the substituted groups may contribute to its efficacy in treating various medical conditions, warranting further research and development in the field of medicinal chemistry.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1H-Imidazole, 2-(3-chlorophenyl)-5-(trifluoroMethyl) is used as a subject of research to explore its potential applications. 1H-IMidazole, 2-(3-chlorophenyl)-5-(trifluoroMethyl)'s unique structure and the possibility of various biological activities make it a valuable target for investigation, potentially leading to the discovery of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 33469-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,6 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 33469-14:
(7*3)+(6*3)+(5*4)+(4*6)+(3*9)+(2*1)+(1*4)=116
116 % 10 = 6
So 33469-14-6 is a valid CAS Registry Number.

33469-14-6SDS

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 2-(3-chloro-phenyl)-4-trifluoromethyl-1(3)H-imidazole

1.2 Other means of identification

Product number -
Other names 1H-IMIDAZOLE, 2-(3-CHLOROPHENYL)-5-(TRIFLUOROMETHYL)-

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:33469-14-6 SDS

33469-14-6Relevant articles and documents

Discovery of novel 2-aryl-4-bis-amide imidazoles (ABAI) as anti-inflammatory agents for the treatment of inflammatory bowel diseases (IBD)

Li, Ling,Yuan, Sijie,Lin, Lin,Yang, Fang,Liu, Ting,Xu, Chenglong,Zhao, Huiting,Chen, Jingxuan,Kuang, Peihua,Chen, Ting,Liao, Wenzhen,Chen, Jianjun

, (2022/01/28)

A series of 2-Aryl-4-Bis-amide Imidazoles (ABAI-1 to 30) were designed as anti-inflammatory agents. These compounds were synthesized and evaluated for the in vitro anti-inflammatory activities (inhibition of NO production and release of inflammatory cytok

Synthesis, structure, and neuroprotective properties of novel imidazolyl nitrones

Dhainaut, Alain,Tizot, André,Raimbaud, Eric,Lockhart, Brian,Lestage, Pierre,Goldstein, Solo

, p. 2165 - 2175 (2007/10/03)

A new series of imidazolyl nitrones spin traps has been synthesized and evaluated pharmacologically. The salient structural feature of these molecules is the presence of an imidazole moiety substituted by aromatic or heteroaromatic cycles. This connectivi

Trifluoromethylimidazoles and a method for their preparation

-

, (2008/06/13)

4(5)-Trifluoromethylimidazoles having optional substituents in the 1 and 2 positions are provided. The novel 4(5)-trifluoromethylimidazoles are prepared by reacting a 1,1-dihalo-3,3,3-trifluoroacetone compound with an appropriate carboxaldehyde and ammoni

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