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Butanedioic acid, 2,3-bis(4-ethoxy-3-methoxybenzoyl)-, diethyl ester is a complex organic compound with the chemical formula C24H28O10. It is a derivative of butanedioic acid, featuring two 4-ethoxy-3-methoxybenzoyl groups attached to the central butanedioic acid structure. The compound is characterized by its ester functional groups, which are formed by the reaction of the carboxylic acid groups of butanedioic acid with ethanol. This results in the formation of diethyl esters, enhancing the compound's solubility and reactivity. The presence of ethoxy and methoxy groups on the benzoyl moieties contributes to its overall polarity and potential applications in various chemical and pharmaceutical processes.

752-00-1

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752-00-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 752-00-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 752-00:
(5*7)+(4*5)+(3*2)+(2*0)+(1*0)=61
61 % 10 = 1
So 752-00-1 is a valid CAS Registry Number.

752-00-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-11H-benzo[b]phenoxazine-6,11(12H)-dione

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

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More Details:752-00-1 SDS

752-00-1Relevant academic research and scientific papers

A novel synthetic route to furan-lignans

Wu, Anxin,Wang, Mingyi,Pan, Xinfu

, p. 2087 - 2091 (2007/10/03)

Three naturally occurring furan-lignans and two analogs have been synthesized by a short and efficient route starting from the corresponding aryl acid. The selective reductive removal of allylic hydroxy by palladium oxide in a mixed solvent of THF-CHCl3 was employed as the key step.

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