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Propanoic acid, 2-methyl-2-[4-(2-phenylethenyl)phenoxy]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52179-16-5

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52179-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52179-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,7 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52179-16:
(7*5)+(6*2)+(5*1)+(4*7)+(3*9)+(2*1)+(1*6)=115
115 % 10 = 5
So 52179-16-5 is a valid CAS Registry Number.

52179-16-5SDS

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 ethyl 2-methyl-2-[4-(2-phenylethenyl)phenoxy]propanoate

1.2 Other means of identification

Product number -
Other names Propanoic acid,2-methyl-2-[4-(2-phenylethenyl)phenoxy]-,ethyl 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:52179-16-5 SDS

52179-16-5Relevant academic research and scientific papers

Effect of stilbene and chalcone scaffolds incorporation in clofibric acid on PPARα agonistic activity

Giampietro, Letizia,D'Angelo, Alessandra,Giancristofaro, Antonella,Ammazzalorso, Alessandra,De Filippis, Barbara,Di Matteo, Mauro,Fantacuzzi, Marialuigia,Linciano, Pasquale,Maccallini, Cristina,Amoroso, Rosa

, p. 59 - 65 (2014/01/17)

In an effort to develop safe and efficacious compounds for the treatment of metabolic disorders, new compounds based on a combination of clofibric acid, the active metabolite of clofibrate, and trans-stilbene, chalcone, and other lipophilic groups were synthesized. They were evaluated for PPARα transactivation activity; all branched derivatives showed an increase of the transcriptional activity of receptor compared to the linear ones. Noteworthy, stilbene and benzophenone branched derivatives activated the PPARα better than clofibric acid.

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