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132017-98-2

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132017-98-2 Usage

General Description

3-(2-HYDROXY-4-METHOXY-PHENYL)-3-OXO-PROPIONIC ACID METHYL ESTER is a chemical compound with the formula C11H12O5. It is a methyl ester derivative of 3-(2-hydroxy-4-methoxy-phenyl)-3-oxo-propionic acid, and it is also known as Ferulic acid methyl ester. It is a natural phenolic compound found in various plant sources and possesses antioxidant and anti-inflammatory properties. 3-(2-HYDROXY-4-METHOXY-PHENYL)-3-OXO-PROPIONIC ACID METHYL ESTER has been studied for its potential health benefits, including its role in protecting cells from oxidative damage and its potential use in skincare products. It is also used in pharmaceutical and cosmetic formulations due to its antioxidant and anti-aging properties.

Check Digit Verification of cas no

The CAS Registry Mumber 132017-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,1 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132017-98:
(8*1)+(7*3)+(6*2)+(5*0)+(4*1)+(3*7)+(2*9)+(1*8)=92
92 % 10 = 2
So 132017-98-2 is a valid CAS Registry Number.

132017-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(2-hydroxy-4-methoxyphenyl)-3-oxopropanoate

1.2 Other means of identification

Product number -
Other names AB1522

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:132017-98-2 SDS

132017-98-2Relevant articles and documents

Synthesis and Protein-Tyrosine Kinase Inhibitory Activities of Flavanoid Analogues

Cushman, Mark,Nagarathnam, Dhanapalan,Burg, Debra L.,Geahlen, Robert L.

, p. 798 - 806 (2007/10/02)

Treatment of o-hydroxyacetophenones 2a-e with excess lithium bis(trimethylsilyl)amide followed by dialkyl carbonates gave 3-(2-hydroxyaryl)-3-oxopropanoates 3a-e.The latter substances were transformed through the reaction of their magnesium chelates with

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