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Ethanediamide, N1,N2-bis(2-methylpropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14040-76-7

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14040-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14040-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,4 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14040-76:
(7*1)+(6*4)+(5*0)+(4*4)+(3*0)+(2*7)+(1*6)=67
67 % 10 = 7
So 14040-76-7 is a valid CAS Registry Number.

14040-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-bis(2-methylpropyl)oxamide

1.2 Other means of identification

Product number -
Other names N,N'-diisobutyl-oxalamide

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:14040-76-7 SDS

14040-76-7Upstream product

14040-76-7Downstream Products

14040-76-7Relevant academic research and scientific papers

Reactivity of Carbamoyl Radicals. A New, General, Convenient Free-Radical Synthesis of Isocyanates from Monoamides of Oxalic Acid

Minisci, Francesco,Fontana, Francesca,Coppa, Fausta,Yan, Yong Ming

, p. 5430 - 5433 (1995)

A new, general, simple synthesis of isocyanates was developed by oxidation of monoamides of oxalix acid with peroxydisulfate catalyzed by Ag and Cu salts.The reaction was carried out in a two-phase system (water and an organic solvent), and it is suitable also for practical applications, due to the simple experimental conditions and the inexpensive as well as nontoxic reagents.The first example of homolytic intramolecular aromatic carbamoylation is also reported.

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