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2-(FluoroMethyl)-1-Methyl-1H-iMidazole is a colorless liquid chemical compound with the molecular formula C5H6FN3. It is a derivative of imidazole, a heterocyclic aromatic organic compound, featuring a fluoromethyl group and a methyl group attached to the imidazole ring. 2-(FluoroMethyl)-1-Methyl-1H-iMidazole is characterized by its faint odor and is utilized as a building block in the synthesis of various drugs and other organic compounds in the pharmaceutical industry.

871507-59-4

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871507-59-4 Usage

Uses

Used in Pharmaceutical Industry:
2-(FluoroMethyl)-1-Methyl-1H-iMidazole is used as a building block for the synthesis of various drugs and organic compounds. Its unique structure allows it to be a valuable component in the development of new pharmaceuticals with potential therapeutic applications.
Used as a Precursor in Antifungal and Antibacterial Agents:
In the field of medicinal chemistry, 2-(FluoroMethyl)-1-Methyl-1H-iMidazole serves as a precursor in the synthesis of antifungal and antibacterial agents. Its incorporation into these agents can enhance their effectiveness against infections caused by fungi and bacteria.
Used in the Development of New Pharmaceuticals and Agrochemicals:
2-(FluoroMethyl)-1-Methyl-1H-iMidazole is also utilized in the development of new pharmaceuticals and agrochemicals. Its versatile chemical properties make it a promising candidate for the creation of innovative compounds with potential applications in medicine and agriculture.
Used as a Reagent in Organic Synthesis:
2-(FluoroMethyl)-1-Methyl-1H-iMidazole is employed as a reagent in organic synthesis, where it can participate in various chemical reactions to form new organic compounds. Its reactivity and stability make it a useful tool in the synthesis of complex organic molecules.
Used as a Research Tool in the Study of Imidazole Derivatives:
2-(FluoroMethyl)-1-Methyl-1H-iMidazole is used as a research tool in the study of imidazole derivatives. Its unique structure allows scientists to investigate the properties and potential applications of imidazole-based compounds, contributing to the advancement of knowledge in organic chemistry and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 871507-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,5,0 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 871507-59:
(8*8)+(7*7)+(6*1)+(5*5)+(4*0)+(3*7)+(2*5)+(1*9)=184
184 % 10 = 4
So 871507-59-4 is a valid CAS Registry Number.

871507-59-4SDS

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 1H-Imidazole, 2-(fluoromethyl)-1-methyl-

1.2 Other means of identification

Product number -
Other names 2-(Fluoromethyl)-1-methyl-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:871507-59-4 SDS

871507-59-4Upstream product

871507-59-4Downstream Products

871507-59-4Relevant academic research and scientific papers

Expedient synthesis of substituted imidazoles from nitriles

Frutos, Rogelio P.,Gallou, Isabelle,Reeves, Diana,Xu, Yibo,Krishnamurthy, Dhileepkumar,Senanayake, Chris H.

, p. 8369 - 8372 (2005)

Expedient and practical new methodology for the synthesis of substituted imidazoles was developed to provide a rapid access to a variety of 2-substituted, 1,2-disubstituted and 1,2,4-trisubstituted imidazoles by the direct CuCl-mediated reaction of nitriles with α-amino acetals in an intermolecular as well as intramolecular fashion.

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