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

190182-03-7

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190182-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 190182-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,1,8 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 190182-03:
(8*1)+(7*9)+(6*0)+(5*1)+(4*8)+(3*2)+(2*0)+(1*3)=117
117 % 10 = 7
So 190182-03-7 is a valid CAS Registry Number.

190182-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-[4-(2-aminoethyl)phenoxy]-2-methylpropanoate

1.2 Other means of identification

Product number -
Other names Propanoic acid,2-[4-(2-aminoethyl)phenoxy]-2-methyl-,methyl 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:190182-03-7 SDS

190182-03-7Relevant academic research and scientific papers

Synthesis, characterization and biological evaluation of ureidofibrate-like derivatives endowed with peroxisome proliferator-activated receptor activity

Porcelli,Gilardi,Laghezza,Piemontese,Mitro,Azzariti,Altieri,Cervoni,Fracchiolla,Giudici,Guerrini,Lavecchia,Montanari,Di Giovanni,Paradiso,Pochetti,Simone,Tortorella,Crestani,Loiodice

, p. 37 - 54 (2012/03/09)

A series of ureidofibrate-like derivatives was prepared and assayed for their PPAR functional activity. A calorimetric approach was used to characterize PPARγ-ligand interactions, and docking experiments and X-ray studies were performed to explain the obs

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