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Benzenepropanoic acid, b-oxo-a-(2-oxo-2-phenylethylidene)-, ethyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84269-41-0

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84269-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84269-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,6 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84269-41:
(7*8)+(6*4)+(5*2)+(4*6)+(3*9)+(2*4)+(1*1)=150
150 % 10 = 0
So 84269-41-0 is a valid CAS Registry Number.

84269-41-0SDS

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-benzoyl-4-oxo-4-phenylbut-2-enoate

1.2 Other means of identification

Product number -
Other names -

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:84269-41-0 SDS

84269-41-0Relevant academic research and scientific papers

Organocatalytic enantioselective conjugate addition of pyrazolin-5-ones to arylomethylidene malonates

Sharma, Arun,Sharma, Vivek,Chimni, Swapandeep Singh

, p. 9514 - 9523 (2019)

An efficient asymmetric organocatalytic conjugate addition reaction of pyrazolin-5-ones with arylomethylidene malonates has been successfully developed by employing bifunctional Cinchona derived thiourea organocatalysts. The protocol provides straightforward access to pyrazole substituted scaffolds in good yields with high stereocontrol.

An Expedient, Direct, Three-Component Approach for the Synthesis of 4-Thioarylpyrroles

Anandan, Sambandam,Neelamegam, Chinnaraj,Rajeshkumar, Venkatachalam

supporting information, p. 4023 - 4033 (2019/10/28)

A three-component strategy for the synthesis of 4-thioarylpyrroles from 1,4-enediones, thiols, and ammonium formate in one-pot has been developed. The reaction proceeds through the sequential thiol-Michael/Paal-Knorr reaction of 1,4-enediones with the for

Heterogeneous synthesis of 1,4-enediones and 1,4-diketones with manganese oxide molecular sieves OMS-2 as a recyclable catalyst

Meng, Xu,Zhang, Jinqi,Chen, Gexin,Chen, Baohua,Zhao, Peiqing

, p. 239 - 242 (2015/07/27)

An efficient manganese oxide octahedral molecular sieves OMS-2-catalyzed chemoselective synthesis of 1,4-enediones and 1,4-diketones from 1,3-dicarbonyls and α-iodoacetophenones is described. The present catalytic system can be applied in one-pot, three-c

Target-oriented synthesis: Miscellaneous synthetic routes to access 1,4-enediones through the coupling of 1,3-dicarbonyl compounds with multiform substrates

Zhu, Yan-Ping,Cai, Qun,Gao, Qing-He,Jia, Feng-Cheng,Liu, Mei-Cai,Gao, Meng,Wu, An-Xin

supporting information, p. 6392 - 6398 (2013/07/25)

Target-oriented synthetic protocol was presented for the synthesis of 1,4-enediones. The approach can efficiently construct 1,4-enediones through different reaction pathways from multiform substrates α-halo aromatic ketones, 2-hydroxy-aromatic ketones and methyl carbinols. In this reaction, CuI was found to be the most efficient catalyst. Multiform substrates were also found to perform well to afford the products in a one-pot fashion.

Formation of unsymmetrical 1,4-enediones via A focusing domino strategy: Cross-coupling of 1,3-dicarbonyl compounds and methyl ketones or terminal aryl alkenes

Gao, Meng,Yang, Yan,Wu, Yan-Dong,Deng, Cong,Cao, Li-Ping,Meng, Xiang-Gao,Wu, An-Xin

supporting information; experimental part, p. 1856 - 1859 (2010/10/03)

A highly efficient synthesis of unsymmetrical 1,4-enediones from 1,3-dicarbonyl compounds and methyl ketones or terminal aryl alkenes has been developed via a focusing domino strategy. Simple and readily available starting materials, mild reaction conditions, and a very simple operation are advantages of the reaction, which allow straightforward synthesis of a variety of unsymmetrical 1,4-enediones.

Stereospecific Stille-coupling reaction of (Z)-1,2- bis(trimethylstannyl)ethenes with hypervalent iodonium salts

Kang, Suk-Ku,Lee, Yong-Tack,Lee, Sang-Ho

, p. 3573 - 3576 (2007/10/03)

The Stille coupling of (Z)-1,2-bis(trimethylstannyl)ethenes with hypervalent iodonium salts (1 equiv) proceeded stereospecifically in the presence of PdCl2 (5 mol %) in DMF at room temperature to afford partially substituted (Z)-vinylstannanes under mild conditions. Alternatively, the use of 2 equivalents of hypervalent iodonium salts afforded tri-substituted alkenes.

Photosensitized Oxidation of Furans. Part 7. Solvent Effects in Thermal Conversion of the endo-Peroxides of Arylfurans

Graziano, M. Liliana,Iesce, M. Rosaria,Chiosi, Sergio,Scarpati, Rachele

, p. 2071 - 2074 (2007/10/02)

Thermal conversion of the endo-peroxides of the arylfurans (1) in a polar aprotic solvent leads to aroylenol esters (4) and diaroyl epoxides (3), the predominance of one over being concentration dependent.The results can be rationalized on the basis of th

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