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Acetamide, 2,2,2-trifluoro-N-[4-(phenylamino)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

162557-83-7

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162557-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162557-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,5,5 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 162557-83:
(8*1)+(7*6)+(6*2)+(5*5)+(4*5)+(3*7)+(2*8)+(1*3)=147
147 % 10 = 7
So 162557-83-7 is a valid CAS Registry Number.

162557-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-anilinophenyl)-2,2,2-trifluoroacetamide

1.2 Other means of identification

Product number -
Other names Acetamide,2,2,2-trifluoro-N-[4-(phenylamino)phenyl]

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:162557-83-7 SDS

162557-83-7Relevant academic research and scientific papers

Potential-dependent nucleophilicity of polyaniline

McCoy, Christopher H.,Lorkovic, Ivan M.,Wrighton, Mark S.

, p. 6934 - 6943 (1995)

The reaction of electrode-confined polyaniline with trifluoroacetic anhydride in acidified acetonitrile giving insulating and electroinactive trifluoroacetylated polyaniline has been studied by electrochemistry, reflectance IR, and microelectrochemistry.

Trifluoroacetylation of amines with trifluoroacetic acid in the presence of trichloroacetonitrile and triphenylphosphine

Kim, Joong-Gon,Jang, Doo Ok

scheme or table, p. 683 - 685 (2010/04/02)

We developed a mild and convenient trifluoroacetylation process for amines using a combination of trichloroacetonitrile and triphenylphosphine. The reaction that we designed is applicable to the trifluoroacetylation of a wide variety of amines, including amines with stereogenic centers, which underwent trifluoroacetylation without racemization.

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