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407-37-4

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407-37-4 Usage

General Description

AcetaMide, 2,2,2-trifluoro-N-(2,2,2-trifluoroethyl)- is a chemical compound with the molecular formula C6H4F6NO. It is a derivative of acetamide with two trifluoroethyl groups attached to the nitrogen atom. AcetaMide, 2,2,2-trifluoro-N-(2,2,2-trifluoroethyl)- is used in various industrial applications, including as a solvent and intermediate in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential use as a reagent in organic chemistry reactions. AcetaMide, 2,2,2-trifluoro-N-(2,2,2-trifluoroethyl)- is considered to be a stable and non-reactive compound under normal conditions, but proper precautions should be taken when handling it due to its potential health and environmental hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 407-37-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 407-37:
(5*4)+(4*0)+(3*7)+(2*3)+(1*7)=54
54 % 10 = 4
So 407-37-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H3F6NO/c5-3(6,7)1-11-2(12)4(8,9)10/h1H2,(H,11,12)

407-37-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoro-N-(2,2,2-trifluoroethyl)acetamide

1.2 Other means of identification

Product number -
Other names Acetamide,2,2,2-trifluoro-N-(2,2,2-trifluoroethyl)

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:407-37-4 SDS

407-37-4Relevant articles and documents

N-Substituted trifluoroacetimidoyl halides: Synthesis and properties

Romanov,Vasil'ev,Zatonsky

, p. 1639 - 1644 (2001)

N-Substituted trifluoroacetimidoyl halides in ionic-type transformations readily undergo nucleophilic substitution and dehydrofluorination rather than 1,3-dehydrohalogenation to give nitrile ylides.

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