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Benzenamine, 4-fluoro-N,N-bis(4-fluorophenyl)-, also known as 4-fluoro-N,N-bis(4-fluorophenyl)aniline or 4,4'-difluorodiphenylamine, is an organic compound with the chemical formula C12H8F2N. It is a derivative of aniline, where two hydrogen atoms on the benzene ring are replaced by fluorine atoms, and the remaining two hydrogen atoms on the nitrogen atom are replaced by 4-fluorophenyl groups. Benzenamine, 4-fluoro-N,N-bis(4-fluorophenyl)- is a white crystalline solid with a melting point of 95-97°C. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its potential applications in the production of fluorinated compounds, it has gained significant interest in the field of organic chemistry.

899-26-3

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899-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 899-26-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 899-26:
(5*8)+(4*9)+(3*9)+(2*2)+(1*6)=113
113 % 10 = 3
So 899-26-3 is a valid CAS Registry Number.

899-26-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluoro-N,N-bis(4-fluorophenyl)aniline

1.2 Other means of identification

Product number -
Other names Tris-<p-fluorphenyl>-amin

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:899-26-3 SDS

899-26-3Downstream Products

899-26-3Relevant academic research and scientific papers

Selective one-pot synthesis of symmetrical and unsymmetrical di- and triarylamines with a ligandless copper catalytic system

Tlili, Anis,Monnier, Florian,Taillefer, Marc

supporting information; experimental part, p. 6408 - 6410 (2012/07/27)

The one-pot synthesis of symmetrical or unsymmetrical di- or triarylamines using aryl iodides or bromides and LiNH2 as ammonia source is reported. This highly selective method is based, for the first time, on a copper-catalyzed system, which does not require the presence of any additional ligand.

Selective palladium-catalyzed arylation of ammonia: Synthesis of anilines as well as symmetrical and unsymmetrical di- and triarylamines

Surry, David S.,Buchwald, Stephen L.

, p. 10354 - 10355 (2008/03/13)

It is shown that by selection of an appropriate palladium/ligand system, temperature, concentration, and stoichiometry of reagents, ammonia may be selectively arylated to give either anilines, symmetrical di-, or triarylamines. Furthermore different aryl halides may be added sequentially to the reaction mixture, allowing the synthesis of unsymmetrical di- and triarylamines from aryl halides and ammonia in a one-pot protocol Copyright

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