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16703-52-9

16703-52-9

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16703-52-9 Usage

General Description

ETHYL N,N-DIMETHYLOXAMATE is a chemical compound with the molecular formula C5H11NO3. It is a clear, colorless liquid that is commonly used as a solvent and reagent in organic synthesis. It is derived from oxamic acid and is commonly used as a protecting group for amines in peptide synthesis. It is also used as a precursor in the production of other organic compounds. ETHYL N,N-DIMETHYLOXAMATE is considered to be relatively stable and non-toxic, with low potential for environmental and health hazards when handled and used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 16703-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,0 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16703-52:
(7*1)+(6*6)+(5*7)+(4*0)+(3*3)+(2*5)+(1*2)=99
99 % 10 = 9
So 16703-52-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO3/c1-4-10-6(9)5(8)7(2)3/h4H2,1-3H3

16703-52-9 Well-known Company Product Price

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  • Alfa Aesar

  • (L08923)  Ethyl N,N-dimethyloxamate, 98%   

  • 16703-52-9

  • 5g

  • 347.0CNY

  • Detail

  • Alfa Aesar

  • (L08923)  Ethyl N,N-dimethyloxamate, 98%   

  • 16703-52-9

  • 25g

  • 1149.0CNY

  • Detail

16703-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(dimethylamino)-2-oxoacetate

1.2 Other means of identification

Product number -
Other names dimethyl-oxalamic acid ethyl ester

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:16703-52-9 SDS

16703-52-9Relevant articles and documents

Donatsch et al.

, p. 1185 (1970)

SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE

-

Paragraph 000667, (2019/06/05)

The present invention provides novel heteroaryl compounds, pharmaceutical acceptable salts and formulations thereof. They are useful in preventing, managing, treating or lessening the severity of a protein kinase-mediated disease. The invention also provides pharmaceutically acceptable compositions comprising such compounds and methods of using the compositions in the treatment of protein kinase-mediated disease.

Synthesis of 2,3-allenylamides utilizing [1,2]-phospha-Brook rearrangement and their application to gold-catalyzed cycloisomerization providing 2-aminofuran derivatives

Kondoh, Azusa,Ishikawa, Sho,Aoki, Takuma,Terada, Masahiro

supporting information, p. 12513 - 12516 (2016/10/24)

An efficient synthetic method for 2,3-allenylamides having an oxygen functionality at the 2-position, which are difficult to access by conventional methods, was newly developed by utilizing the [1,2]-phospha-Brook rearrangement under Br?nsted base catalysis. Further manipulation of the 2,3-allenylamides via gold-catalyzed cycloisomerization enables the formation of 2-aminofuran derivatives.

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