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ethyl 3-(4-ethoxyphenyl)-3-oxopropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51725-83-8

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51725-83-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51725-83-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,7,2 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51725-83:
(7*5)+(6*1)+(5*7)+(4*2)+(3*5)+(2*8)+(1*3)=118
118 % 10 = 8
So 51725-83-8 is a valid CAS Registry Number.

51725-83-8SDS

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 Ethyl 3-(4-ethoxyphenyl)-3-oxopropanoate

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:51725-83-8 SDS

51725-83-8Downstream Products

51725-83-8Relevant academic research and scientific papers

Synthesis and herbicidal evaluation of novel 3-[(α-hydroxy- substituted)benzylidene]pyrrolidine-2,4-diones

Zhu, Youquan,Zou, Xiaomao,Hu, Fangzhong,Yao, Changsheng,Liu, Bin,Yang, Huazheng

, p. 9566 - 9570 (2007/10/03)

A series of 3-[(α-hydroxy-substituted) benzylidene]pyrrolidine-2,4- dione derivatives were synthesized as candidate herbicides by reacting different aroyl acetates with N-substituted glycine esters. The new compounds were identified by 1H NMR spectroscopy and elemental analyses. Their herbicidal activities were evaluated. Some compounds exhibited excellent herbicidal activities at a dose of 187.5 g/ha. A suitable electron-donating substituent at the 2- and/or 4-position of the phenyl ring was essential for high herbicidal activity, a result that has not been reported before. It was also found that the title compound's structure-activity relationships were different from those of other similar kinds of earlier compounds, a result that may depend on the enol structure difference.

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