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Pentanedioic acid, 3,3-diphenyl-, diethyl ester, also known as diethyl 3,3-diphenylglutarate, is an organic compound with the chemical formula C17H18O4. It is a colorless to pale yellow liquid with a molecular weight of 290.32 g/mol. This ester is derived from pentanedioic acid (glutaric acid) and features two phenyl groups attached to the third carbon of the pentane backbone. Diethyl 3,3-diphenylglutarate is synthesized by the esterification of 3,3-diphenylglutaric acid with ethanol, resulting in the formation of an ester linkage between the carboxylic acid group and the ethanol molecule. Pentanedioic acid, 3,3-diphenyl-, diethyl ester is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the production of polymers and as a reagent in organic synthesis.

3531-26-8

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3531-26-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3531-26-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,3 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3531-26:
(6*3)+(5*5)+(4*3)+(3*1)+(2*2)+(1*6)=68
68 % 10 = 8
So 3531-26-8 is a valid CAS Registry Number.

3531-26-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-Diphenylglutarsaeure-diethylester

1.2 Other means of identification

Product number -
Other names diethyl 3,3-diphenylglutarate

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:3531-26-8 SDS

3531-26-8Relevant academic research and scientific papers

Regio- and Stereoselectivity of the Hydrocarbonylating Cyclization of 1,4-Dienes with Carbon Monoxide: Synthesis of (+/-)-(α)-Cuparenone

Eilbracht, Peter,Balss, Erika,Acker, Michael

, p. 825 - 839 (2007/10/02)

Directed towards the synthesis of the cuparene skeleton the hydrocarbonylating cyclization of 1,4-dienes 16, 27 to form cyclopentanones 17, 28 was tested for its regio- and stereoselectivity as well as the toleration of aryl groups in this cyclization met

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