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2-Propenoic acid, 3-(benzoyloxy)-3-phenyl-, ethyl ester, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65847-84-9

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65847-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65847-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,4 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65847-84:
(7*6)+(6*5)+(5*8)+(4*4)+(3*7)+(2*8)+(1*4)=169
169 % 10 = 9
So 65847-84-9 is a valid CAS Registry Number.

65847-84-9SDS

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 β-benzoyloxy-cinnamic acid ethyl ester

1.2 Other means of identification

Product number -
Other names Ethyl β-Benzoxycinnamat

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:65847-84-9 SDS

65847-84-9Relevant academic research and scientific papers

Direct oxidative esterification of toluene with 1,3-dicarbonyl compounds catalysed by copper complex supported on magnetic nanoparticles

Azizi, Kobra,Esfandiary, Naghmeh,Karimi, Meghdad,Kazemi, Maryam,Heydari, Akbar

, (2017/07/25)

Toluene oxidation is one of the substantial industrial technologies since oxidized products are industrially very important intermediates. A Fe3O4@cysteine@Cu-catalysed reaction that uses tert-butyl hydroperoxide as oxidant to produce esters from toluene and β-diketones or β-keto esters, enolate precursors, has been developed. Oxidative esterification of toluene with 1,3-dicarbonyl derivatives led to C─O bond formation and direct C─H functionalization.

Oxidative esterification of methylarenes and 1,3-dicarbonyls catalysed by copper chloride immobilized on magnetic nanoparticles

Nakisa, Athar,Karimi, Meghdad,Yazdani, Elahe,Heydari, Akbar

, (2017/07/25)

Superparamagnetic CuCl nanoparticles were prepared and identified as an effective heterogeneous catalyst for the tandem transformation of methylarenes and 1,3-dicarbonyl compounds into the corresponding enole esters by the use of tert-butyl hydroperoxide as an external oxidant. The catalyst can be removed from the reaction medium simply by use of an external magnet. As a consequence, various derivatives of enol esters were synthesized in moderate to good yields.

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