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N-[4-(TRIFLUOROMETHYL)PHENYL]-4-FLUOROBENZAMIDE is a complex organic compound with the molecular formula C14H8F4N2O. It is characterized by the presence of a benzamide group, which consists of a benzene ring attached to a carboxamide functional group. The compound features a 4-fluorobenzene ring and a 4-(trifluoromethyl)phenyl group, which are connected through the amide linkage. The trifluoromethyl group adds to the molecule's stability and lipophilicity, while the fluorine atoms can influence the compound's electronic properties and reactivity. This chemical is often used in the synthesis of pharmaceuticals and agrochemicals due to its potential to form stable and biologically active molecules.

2054-01-5

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2054-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2054-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2054-01:
(6*2)+(5*0)+(4*5)+(3*4)+(2*0)+(1*1)=45
45 % 10 = 5
So 2054-01-5 is a valid CAS Registry Number.

2054-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluoro-N-[4-(trifluoromethyl)phenyl]benzamide

1.2 Other means of identification

Product number -
Other names 4-FLUORO-4'-(TRIFLUOROMETHYL)BENZANILIDE

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:2054-01-5 SDS

2054-01-5Downstream Products

2054-01-5Relevant academic research and scientific papers

Experimental and computational analysis of supramolecular motifs involving Csp2(aromatic)-F and CF3 groups in organic solids

Panini, Piyush,Gonnade, Rajesh G.,Chopra, Deepak

, p. 4981 - 5001 (2016/07/06)

A detailed experimental (SCXRD) and theoretical (PIXEL and QTAIM) investigation of the evolution of different supramolecular motifs formed via the presence of both C(sp2)/(sp3)-F groups in the crystal packing has been performed in a

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