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Hydrazinecarboxylic acid, 2,2-dimethyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55741-07-6

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55741-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55741-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,4 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55741-07:
(7*5)+(6*5)+(5*7)+(4*4)+(3*1)+(2*0)+(1*7)=126
126 % 10 = 6
So 55741-07-6 is a valid CAS Registry Number.

55741-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N-(dimethylamino)carbamate

1.2 Other means of identification

Product number -
Other names methyl dimethylcarbazate

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:55741-07-6 SDS

55741-07-6Downstream Products

55741-07-6Relevant academic research and scientific papers

Photolysis of Dimethylcarbamoyl Azide in the Presence of a Cyclic Aminimide

Gibson, Harry H.,Weissinger, Keith,Abashawl, Aida,Hall, Greg,Lawshae, Tom,et al.

, p. 3858 - 3861 (2007/10/02)

Dimethylcarbamoyl azide has been photolyzed in the presence of methyl isocyanate to produce the cyclic aminimide 1,1,4-trimethyl-1,2,4-triazolidine-3,5-dione 1,2-ylide (6) and the azo compound N-(dimethylcarbamoyl)-N,N'N'-trimethylazodicarboxamide (7).The azo compound 7 arises a photolytic reaction between dimethylcarbamoyl azide and aminimide 6.Mechanistic studies support a reaction path involving intermolecular-assisted loss of nitrogen from the azide as a result of interaction with aminimide 6.

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