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Acetamide, N,N'-1,2-ethanediylbis[2,2,2-trifluoro-N-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61553-61-5

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61553-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61553-61-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,5 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61553-61:
(7*6)+(6*1)+(5*5)+(4*5)+(3*3)+(2*6)+(1*1)=115
115 % 10 = 5
So 61553-61-5 is a valid CAS Registry Number.

61553-61-5SDS

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 2,2,2-trifluoro-N-methyl-N-[2-[methyl-(2,2,2-trifluoroacetyl)amino]ethyl]acetamide

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61553-61-5 SDS

61553-61-5Downstream Products

61553-61-5Relevant articles and documents

Acid-Catalyzed Ring-Chain Tautomerism in 1,3-Diazolidines

Lambert, Joseph B.,Wang, Gen-tai,Huseland, Dave E.,Takiff, Larry C.

, p. 68 - 71 (1987)

Ring-chain tautomerism has been studied in 2-substituted and 1,3-disubstituted diazolidines.In trifluoroacetic acid, these heterocycles are in equilibrium with the open-chain iminium ion.For materials lacking 2 substitution, 5-10percent of the chain form is present at room temperature.Because of resonance stabilization of the positive charge, 2-aryl-substituted systems have about 30percent of the chain form.All of these ring and chain forms undergo interconversion on the NMR time scale with a free energy of activation of 16 - 18 kcal/mol.

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