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1H-Imidazole, 2-(2-furanyl)-5-(trifluoroMethyl)is a chemical compound that belongs to the class of imidazole derivatives. It features a furanyl group and a trifluoromethyl group attached to the imidazole ring, which endows it with unique structural and reactivity properties. 1H-IMidazole, 2-(2-furanyl)-5-(trifluoroMethyl)holds potential for various biological and pharmaceutical applications, making it a valuable building block for the synthesis of pharmaceuticals and agrochemicals.

33468-88-1

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33468-88-1 Usage

Uses

Used in Pharmaceutical Industry:
1H-Imidazole, 2-(2-furanyl)-5-(trifluoroMethyl)is used as a building block for the synthesis of various pharmaceuticals due to its unique structure and reactivity. Its incorporation into drug molecules can potentially enhance their therapeutic effects and target specific biological pathways.
Used in Agrochemical Industry:
In the agrochemical industry, 1H-Imidazole, 2-(2-furanyl)-5-(trifluoroMethyl)is utilized as a key component in the development of new agrochemicals. Its unique chemical properties can contribute to the creation of more effective and targeted pesticides or other agricultural chemicals.
Used in Antifungal Applications:
1H-Imidazole, 2-(2-furanyl)-5-(trifluoroMethyl)has been studied for its potential antifungal properties, making it a promising candidate for the development of new antifungal agents. Its ability to target and inhibit fungal growth can be harnessed to create more effective treatments for fungal infections.
Used in Antiviral Applications:
1H-IMidazole, 2-(2-furanyl)-5-(trifluoroMethyl)has also shown potential in antiviral research, suggesting its use as an antiviral agent. The incorporation of 1H-Imidazole, 2-(2-furanyl)-5-(trifluoroMethyl)into antiviral drugs could potentially lead to the development of new therapies for viral infections.
Used in Anticancer Applications:
1H-Imidazole, 2-(2-furanyl)-5-(trifluoroMethyl)has been investigated for its potential anticancer properties, indicating its use in the development of novel anticancer drugs. Its ability to target and inhibit cancer cell growth and proliferation could contribute to the creation of more effective cancer treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 33468-88-1 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 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33468-88:
(7*3)+(6*3)+(5*4)+(4*6)+(3*8)+(2*8)+(1*8)=131
131 % 10 = 1
So 33468-88-1 is a valid CAS Registry Number.

33468-88-1SDS

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-Furan-2-yl-5-trifluoromethyl-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2-(2-FURANYL)-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:33468-88-1 SDS

33468-88-1Relevant academic research and scientific papers

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

Synthesis and Cardiotonic Activity of Novel Biimidazoles

Matthews, Donald P.,McCarthy, James R.,Whitten, Jeffrey P.,Kastner, Philip R.,Barney, Charlotte L.,et al.

, p. 317 - 327 (2007/10/02)

A series of substituted 2,2-bi-1H-imidazoles and related analogues was synthesized and evaluated for inotropic activity.Structure-activity relationship studies based on a nonclassical bioisosteric approach indicated the necessity of a cyano group on one o

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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