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(E)-Methyl-4-(3-bromophenyl)-2-oxobut-3-enoate is a chemical compound with the molecular formula C11H9BrO3. It is a derivative of the compound 4-hydroxy-2-nonenal, which is a lipid peroxidation product known to be involved in various pathological processes.

104094-31-7

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104094-31-7 Usage

Uses

Used in Pharmaceutical Industry:
(E)-Methyl-4-(3-bromophenyl)-2-oxobut-3-enoate is used as a versatile building block in the synthesis of pharmaceuticals for its potential pharmacological activity, such as anti-inflammatory and anti-tumor properties.
Used in Agrochemical Industry:
(E)-Methyl-4-(3-bromophenyl)-2-oxobut-3-enoate is used as a building block in the synthesis of agrochemicals, contributing to the development of biologically active compounds for agricultural applications.
Used in Organic Synthesis:
(E)-Methyl-4-(3-bromophenyl)-2-oxobut-3-enoate is used as a reagent in organic synthesis for the preparation of various heterocyclic compounds, expanding its utility in the creation of diverse chemical entities.

Check Digit Verification of cas no

The CAS Registry Mumber 104094-31-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,9 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104094-31:
(8*1)+(7*0)+(6*4)+(5*0)+(4*9)+(3*4)+(2*3)+(1*1)=87
87 % 10 = 7
So 104094-31-7 is a valid CAS Registry Number.

104094-31-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl (3E)-4-(3-bromophenyl)-2-oxo-3-butenoate

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:104094-31-7 SDS

104094-31-7Relevant academic research and scientific papers

Facile synthesis of substituted diaryl sulfones: Via a [3 + 3] benzannulation strategy

Tang, Xiang-Zheng,Tong, Lang,Liang, Hua-Ju,Liang, Jie,Zou, Yong,Zhang, Xue-Jing,Yan, Ming,Chan, Albert S. C.

, p. 3560 - 3563 (2018/05/26)

A base-mediated [3 + 3] benzannulation strategy for the conversion of 1,3-bis(sulfonyl)propenes and β,γ-unsaturated α-ketoesters to diaryl sulfones has been developed. This method provides facile, metal-free and efficient access to highly substituted diaryl sulfones in good to excellent yields. In addition, the sulfonyl group could be easily removed or converted to other functional groups via an organostannane intermediate.

4,5-DIHYDRO-1H-PYRAZOLE DERIVATIVE OR SALTS THEREOF, AND PHARMACEUTICAL COMPOSITION COMPRISING SAME

-

Paragraph 0234; 0235, (2015/11/16)

The present invention provides a 4,5-dihydro-1H-pyrazole derivative or its pharmaceutically acceptable salt, a process for the preparation thereof, and a pharmaceutical composition comprising the same. The 4,5-dihydro-1H-pyrazole derivative or its pharmaceutically acceptable salt effectively increases the LXR transcriptional activity, and therefore can be usefully applied for preventing or treating a dysfunction in cholesterol metabolism, such as cholesterol gallstone, hyperlipidemia, or coronary atherosclerosis.

A New Strategy for Enantioselective Construction of Multisubstituted Five-Membered Oxygen Heterocycles via a Domino Michael/Hemiketalization Reaction

Hua, Yuan-Zhao,Liu, Meng-Meng,Huang, Pei-Jin,Song, Xixi,Wang, Min-Can,Chang, Jun-Biao

supporting information, p. 11994 - 11998 (2015/08/18)

A new highly enantioselective domino Michael/hemiketalization reaction of α-hydroxyacetophenone with β,γ-unsaturated α-keto esters for the synthesis of 2,2,4,5-tetrasubstituted chiral tetrahydrofurans is reported. With 2 mol% intramolecular dinuclear zinc

Organocatalytic Functionalization of carboxylic acids: Isothiourea- catalyzed asymmetric intra- and intermolecular Michael addition-lactonizations

Belmessieri, Dorine,Morrill, Louis C.,Simal, Carmen,Slawin, Alexandra M. Z.,Smith, Andrew D.

, p. 2714 - 2720 (2011/04/23)

Tetramisole promotes the catalytic asymmetric intramolecular Michael addition-lactonization of a variety of enone acids, giving carbo- and heterocyclic products with high diastereo- and enantiocontrol (up to 99:1 dr, up to 99% ee) that are readily derivatized to afford functionalized indene and dihydrobenzofuran carboxylates. Chiral isothioureas also promote the catalytic asymmetric intermolecular Michael addition-lactonization of arylacetic acids and α-keto-β,γ-unsaturated esters, giving anti-dihydropyranones with high diastereo- and enantiocontrol (up to 98:2 dr, up to 99% ee).

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