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Ethyl N-(2,3-dimethylphenyl)glycinate is an organic compound with the chemical formula C12H15NO2. It is a derivative of glycine, an amino acid, and features a 2,3-dimethylphenyl group attached to the nitrogen atom. ethyl N-(2,3-dimethylphenyl)glycinate is a white crystalline solid and is soluble in organic solvents. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. The compound is also known for its potential applications in the development of new materials and as a research tool in chemical and biological studies.

2345-06-4

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2345-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2345-06-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,4 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2345-06:
(6*2)+(5*3)+(4*4)+(3*5)+(2*0)+(1*6)=64
64 % 10 = 4
So 2345-06-4 is a valid CAS Registry Number.

2345-06-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(2,3-dimethylanilino)acetate

1.2 Other means of identification

Product number -
Other names N-<2,3-Dimethyl-phenyl>-glycin-aethylester

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 -
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More Details:2345-06-4 SDS

2345-06-4Relevant academic research and scientific papers

Bromination of Sydnones. I. Reaction with 3-Arylsydnones Containing Electron-Donors on the Aryl Ring

Turnbull, Kenneth

, p. 965 - 968 (2007/10/02)

Bromination has been examined for a series of 3-arylsydnones (1) with electron donors (dimethyl to dimethoxy) on the aryl ring.In no example was exclusive aryl ring bromination observed, however, exclusive sydnone ring bromination could be realized in every case.For two dimethoxyphenyl examples both aryl and sydnone ring bromination occurred.

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