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7497-89-4

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7497-89-4 Usage

General Description

3-Phenoxy propanoic acid methyl ester is a chemical compound that is commonly used as an intermediate in the synthesis of various organic compounds. It is a methyl ester of 3-phenoxypropanoic acid, which is a carboxylic acid with a phenyl group attached to the third carbon atom. 3-PHENOXY PROPANOIC ACID METHYL ESTER is commonly used in the production of pesticides, herbicides, and insecticides due to its ability to inhibit the growth of certain plants and insects. It is also used as a chemical intermediate in the pharmaceutical and agrochemical industries. 3-PHENOXY PROPANOIC ACID METHYL ESTER is considered to be of low toxicity, but proper safety precautions should be taken when handling it.

Check Digit Verification of cas no

The CAS Registry Mumber 7497-89-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7497-89:
(6*7)+(5*4)+(4*9)+(3*7)+(2*8)+(1*9)=144
144 % 10 = 4
So 7497-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-12-10(11)7-8-13-9-5-3-2-4-6-9/h2-6H,7-8H2,1H3

7497-89-4SDS

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 methyl 3-phenoxypropanoate

1.2 Other means of identification

Product number -
Other names 3-Phenoxy-propionsaeure-methylester

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:7497-89-4 SDS

7497-89-4Relevant articles and documents

Palladium-catalyzed aerobic regio- and stereo-selective olefination reactions of phenols and acrylates: Via direct dehydrogenative C(sp2)-O cross-coupling

Wu, Yun-Bin,Xie, Dan,Zang, Zhong-Lin,Zhou, Cheng-He,Cai, Gui-Xin

supporting information, p. 4437 - 4440 (2018/05/03)

An efficient olefination protocol for the oxidative dehydrogenation of phenols and acrylates has been achieved using a palladium catalyst and O2 as the sole oxidant. This reaction exhibits high regio- and stereo-selectivity (E-isomers) with mod

METHOD OF TREATING POLYCYSTIC KIDNEY DISEASES WITH CERAMIDE DERIVATIVES

-

Paragraph 0189, (2016/10/08)

PROBLEM TO BE SOLVED: To provide a method of treating polycystic kidney diseases with ceramide derivatives. SOLUTION: A pharmaceutical composition for treating polycystic kidney disease in a subject comprises an effective amount of a predetermined compoun

Catalytic Olefin hydroalkoxylation by nano particles of pollucite

Zamanian, Sara,Kharat, Ali Nemati

, p. 981 - 986 (2015/06/25)

The catalytic hydroalkoxylation of α,β-unsaturated esters, nitriles, and ethers with aliphatic and aromatic alcohols over pollucite using thermal and microwave-assisted methods was investigated. To study the effect of the alcohol structures on the mechanism of the hydroalkoxylation reaction, different alcohols, such as methanol to butanol, cyclohexanol, phenol, and 2-ethylhexanol were used. The activities of pollucite, in contrast to other basic solids, were scarcely affected by the presence of air and moisture. The correlation between alcohol acidity and reaction activity is discussed. The prepared pollucite was characterized by X-ray diffraction, volumetric nitrogen adsorption surface area analysis, and CO2 temperature-programmed desorption. Scanning electron microscopy analysis revealed that the size of the modified nano catalyst particles was under 40nm.

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