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1H-Imidazole, 2-(3-methylphenyl)-5-(trifluoromethyl)-, is a chemical compound with the molecular formula C11H10F3N. It is an imidazole derivative featuring a trifluoromethyl group and a 3-methylphenyl group attached to the imidazole ring. 1H-IMidazole, 2-(3-Methylphenyl)-5-(trifluoroMethyl)has been investigated for its potential pharmaceutical properties, particularly as an antifungal and antibacterial agent. Its unique chemical and physical properties, conferred by the trifluoromethyl group, make it a promising candidate for further research and development in various fields, including organic chemistry where it can serve as a building block for synthesizing other compounds.

33469-19-1

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33469-19-1 Usage

Uses

Used in Pharmaceutical Industry:
1H-Imidazole, 2-(3-methylphenyl)-5-(trifluoromethyl)is used as an antifungal agent for its potential to combat fungal infections by inhibiting essential fungal processes, thereby disrupting their growth and survival.
1H-Imidazole, 2-(3-methylphenyl)-5-(trifluoromethyl)is also used as an antibacterial agent, leveraging its ability to interfere with bacterial cell functions, which can lead to the inhibition of bacterial growth and help in treating bacterial infections.
Used in Organic Chemistry:
1H-Imidazole, 2-(3-methylphenyl)-5-(trifluoromethyl)serves as a building block in organic chemistry for the synthesis of other complex organic compounds, taking advantage of its reactive sites and the unique properties introduced by the trifluoromethyl group.
Used in Research and Development:
1H-IMidazole, 2-(3-Methylphenyl)-5-(trifluoroMethyl)is utilized in research and development settings to explore its unique chemical and physical properties, with the trifluoromethyl group potentially offering novel reactivity and selectivity in various chemical reactions and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 33469-19-1 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 33469-19:
(7*3)+(6*3)+(5*4)+(4*6)+(3*9)+(2*1)+(1*9)=121
121 % 10 = 1
So 33469-19-1 is a valid CAS Registry Number.

33469-19-1SDS

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-m-tolyl-4-trifluoromethyl-1(3)H-imidazole

1.2 Other means of identification

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

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:33469-19-1 SDS

33469-19-1Downstream Products

33469-19-1Relevant academic research and scientific papers

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

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

2-Pyrazinyl-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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