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53483-66-2

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53483-66-2 Usage

General Description

1-Methyl-5-trifluoromethylbenzimidazole is a chemical compound with the molecular formula C9H7F3N2. It is a benzimidazole derivative with a methyl group and a trifluoromethyl group attached to the carbon atoms. 1-METHYL-5-TRIFLUOROMETHYLBENZIMIDAZOLE is primarily used as a building block for the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It has applications in the pharmaceutical industry for the development of new drugs, and in the agricultural industry for the production of pesticides and herbicides. The trifluoromethyl group in this compound can also impart desirable properties, such as increased lipophilicity and metabolic stability, in drug development and design. Overall, 1-methyl-5-trifluoromethylbenzimidazole is an important intermediate in organic synthesis with various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 53483-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,8 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53483-66:
(7*5)+(6*3)+(5*4)+(4*8)+(3*3)+(2*6)+(1*6)=132
132 % 10 = 2
So 53483-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F3N2/c1-14-5-13-7-4-6(9(10,11)12)2-3-8(7)14/h2-5H,1H3

53483-66-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-5-(trifluoromethyl)benzimidazole

1.2 Other means of identification

Product number -
Other names 3-Methyl-5-trifluoromethylbenzimidazol

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:53483-66-2 SDS

53483-66-2Downstream Products

53483-66-2Relevant articles and documents

Cu-Catalyzed C-H Allylation of Benzimidazoles with Allenes

Dong, Yaxi,Breit, Bernhard

supporting information, p. 6765 - 6769 (2021/09/11)

CuH-catalyzed intramolecular cyclization and intermolecular allylation of benzimidazoles with allenes have been described. The reaction proceeded smoothly with the catalytic system of Cu(OAc)2/Xantphos and catalytic amount of (MeO)2MeSiH. This protocol features mild reaction conditions and a good tolerance of substrates bearing electron-withdrawing, electron-donating, or electron-neutral groups. A new catalytic mechanism was proposed for this copper hydride catalytic system.

2-(4-ARYL-1H-IMIDAZOL-1-YL)ANILINE COMPOUNDS

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Paragraph 0069; 0103, (2015/11/27)

The present invention provides compounds that are useful as vaccine adjuvants and/or antitumor agents and methods for producing and using the same. In one particular aspect of the invention, compounds of the invention are of the formula (I) where R1, R2, R3 and Ar1 are those defined herein.

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