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2-(p-Trifluoromethylbenzyl)-2-imidazoline is a complex organic compound with the molecular formula C10H10F3N2. It is a derivative of imidazoline, featuring a benzyl group substituted with a trifluoromethyl group at the para position. This chemical is known for its potential applications in pharmaceuticals and as a precursor in the synthesis of various compounds. Its structure provides unique properties, such as increased lipophilicity due to the presence of the trifluoromethyl group, which can influence its biological activity and interactions with target proteins. The compound is typically synthesized through a series of chemical reactions and is used in research and development for its potential therapeutic applications.

3038-60-6

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3038-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3038-60-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,3 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3038-60:
(6*3)+(5*0)+(4*3)+(3*8)+(2*6)+(1*0)=66
66 % 10 = 6
So 3038-60-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H11F3N2/c12-11(13,14)9-3-1-8(2-4-9)7-10-15-5-6-16-10/h1-4H,5-7H2,(H,15,16)

3038-60-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[4-(trifluoromethyl)phenyl]methyl]-4,5-dihydro-1H-imidazole

1.2 Other means of identification

Product number -
Other names -

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

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More Details:3038-60-6 SDS

3038-60-6Downstream Products

3038-60-6Relevant academic research and scientific papers

A novel synthetic method for 2-arylmethyl substituted imidazolines and imidazoles from 2-aryl-1,1-dibromoethenes

Huh, Dal Ho,Ryu, Hoejin,Kim, Young Gyu

, p. 9857 - 9862 (2007/10/03)

Various 2-arylmethylimidazolines were prepared by treating readily available 2-aryl-1,1-dibromoethenes with ethylenediamine under mild conditions and further converted into the corresponding imidazoles smoothly with Swern oxidation. Graphical Abstract

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