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4-methyl-2-(trifluoromethyl)-1H-Imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66675-23-8

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66675-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66675-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,7 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66675-23:
(7*6)+(6*6)+(5*6)+(4*7)+(3*5)+(2*2)+(1*3)=158
158 % 10 = 8
So 66675-23-8 is a valid CAS Registry Number.

66675-23-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methyl-2-(trifluoromethyl)-1H-imidazole

1.2 Other means of identification

Product number -
Other names 4-Methyl-2-trifluormethylimidazol

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:66675-23-8 SDS

66675-23-8Relevant academic research and scientific papers

HETEROCYCLIC MODULATORS OF LIPID SYNTHESIS AND COMBINATIONS THEREOF

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Page/Page column 102, (2015/07/07)

Heterocyclic modulators of lipid synthesis are provided as well as pharmaceutically acceptable salts thereof; pharmaceutical compositions comprising such compounds; and methods of treating conditions characterized by disregulation of a fatty acid synthase pathway by the administration of such compounds and combinations of such compounds and other therapeutic agents.

HETEROCYCLIC MODULATORS OF LIPID SYNTHESIS

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Page/Page column 87, (2014/01/18)

Heterocyclic modulators of lipid synthesis are provided as well as pharmaceutically acceptable salts thereof; pharmaceutical compositions comprising such compounds; and methods of treating conditions characterized by disregulation of a fatty acid synthase pathway by the administration of such compounds.

Gold(I)-catalyzed aminohalogenation of fluorinated N′-aryl-N- propargyl amidines for the synthesis of imidazole derivatives under mild conditions

Li, Shan,Li, Zhengke,Yuan, Yafen,Li, Yajun,Zhang, Lisi,Wu, Yongming

, p. 1496 - 1501 (2013/03/14)

A procedure for the synthesis of fluorinated imidazole derivatives from propargyl amidines has been developed. Under gold(I) catalysis, propargyl amidines were converted into 5-fluoromethyl imidazoles in the presence of Selectfluor through a cascade cyclization/fluorination process. In contrast, imidazole-5-carbaldehydes were obtained in high yields when N-iodosuccinimide (NIS) was used as the halogenating reagent. The polarity of the solvent and light had significant impact on the formation of the carbaldehydes. These transformations showed excellent functional-group tolerance. An unfluorinated substrate with an electron-withdrawing group also underwent aminohalogenation to give the corresponding product in good yield. Mechanistic investigation revealed the general pathways of these transformations. Copyright

Photochemical Perfluoroalkylation of Imidazoles

Kimoto, Hiroshi,Fujii, Shozo,Cohen, Louis A.

, p. 2867 - 2872 (2007/10/02)

Imidazole and its derivatives undergo facile trifluoromethylation or perfluoroalkylation, in methanol solution at ambient temperature, following radical dissociation of RFI by γ or UV irradiation.In the case of imidazole, attack occurs preferen

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