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Benzenepropanoic acid, 4-chloro-α-(phenylsulfonyl)-, ethyl ester is a complex organic compound with the chemical formula C16H15ClO4S. It is a derivative of benzenepropanoic acid, featuring a 4-chloro substituent and a phenylsulfonyl group attached to the α-carbon. The ethyl ester functional group is present, indicating that the carboxylic acid group has been esterified with ethanol. Benzenepropanoic acid, 4-chloro-a-(phenylsulfonyl)-, ethyl ester is characterized by its aromatic structure, which includes a benzene ring and a propanoic acid chain. It is likely to be used in the synthesis of pharmaceuticals or other organic compounds due to its unique structure and functional groups.

144076-86-8

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144076-86-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144076-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,0,7 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 144076-86:
(8*1)+(7*4)+(6*4)+(5*0)+(4*7)+(3*6)+(2*8)+(1*6)=128
128 % 10 = 8
So 144076-86-8 is a valid CAS Registry Number.

144076-86-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Benzenesulfonyl-3-(4-chloro-phenyl)-propionic acid ethyl ester

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

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More Details:144076-86-8 SDS

144076-86-8Downstream Products

144076-86-8Relevant academic research and scientific papers

Solid-liquid phase transfer catalytic synthesis V III: The rapid alkylation of ethyl phenylsulfonylacetate under microwave irradiation

Wang,Jiang

, p. 2287 - 2291 (2007/10/02)

Rapid alkylations of ethyl phenylsufonylacetate with a series of halides were performed in 960 W domestic microwave oven, and the isolated yield of α-monoalkylated product varying from 76 to 86%.

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