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Propanedioic acid, bis(2,6-dimethylphenyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60179-55-7

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60179-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60179-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,7 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60179-55:
(7*6)+(6*0)+(5*1)+(4*7)+(3*9)+(2*5)+(1*5)=117
117 % 10 = 7
So 60179-55-7 is a valid CAS Registry Number.

60179-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2,6-dimethylphenyl) propanedioate

1.2 Other means of identification

Product number -
Other names malonic acid bis-(2,6-dimethyl-phenyl ester)

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:60179-55-7 SDS

60179-55-7Relevant academic research and scientific papers

Enantioselective Construction of Single and Vicinal All-Carbon Quaternary Stereocenters through Ion-Pair-Catalyzed 1,6-Conjugate Addition

Zhu, Yasheng,Wang, Hongliang,Wang, Gang,Wang, Zehua,Liu, Zhaopeng,Liu, Lei

supporting information, p. 7248 - 7253 (2021/09/14)

An asymmetric 1,6-conjugate addition to presynthesized δ-aryl-δ-cyano-disubstituted para-quinone methides through bifunctional phosphonium-amide-promoted ion-pair catalysis for acyclic all-carbon quaternary stereocenter construction has been described. Both acyclic and cyclic 1,3-dicarbonyls participate in the asymmetric alkylation reaction, furnishing a wide array of diarylmethanes bearing a single acyclic quaternary carbon stereocenter or vicinal cyclic and acyclic quaternary carbon stereocenters with high efficiency and excellent stereoselectivity. Computational studies elucidate the origin of the enantioselectivity.

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