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α-Bromo-4'-methyl-chalcone is a synthetic organic compound characterized by its molecular formula C15H13BrO. It is a chalcone derivative, which is a type of flavonoid, and is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals. α-bromo-4'-methyl-chalcone features a bromine atom attached to the α-carbon and a methyl group at the 4' position of the chalcone structure. Due to its unique chemical properties, α-bromo-4'-methyl-chalcone can be used as an intermediate in the preparation of other compounds, such as pharmaceuticals with potential therapeutic applications. Its chemical structure and reactivity make it a valuable building block in organic synthesis, particularly in the development of new molecules with specific biological activities.

50603-93-5

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50603-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50603-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,0 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50603-93:
(7*5)+(6*0)+(5*6)+(4*0)+(3*3)+(2*9)+(1*3)=95
95 % 10 = 5
So 50603-93-5 is a valid CAS Registry Number.

50603-93-5Relevant academic research and scientific papers

Modular access to 1,2-allenyl ketones based on a photoredox-catalysed radical-polar crossover process

Du, Chan,Fang, Jianghua,Fang, Yewen,Lei, Wan,Li, Yan,Liu, Yongjun

, p. 8502 - 8506 (2021/10/20)

Herein, a new protocol dealing with the preparation of 1,2-allenyl ketones has been successfully developedviathe reactions of enynes with radicals enabled by dual photoredox/copper catalysis. Based on the results of a deuteration experiment and the competition reaction between cyclopropanation and allenation, the mechanism based on a photoredox-neutral-catalysed radical-polar crossover process has been proposed. Synthetic applications of allenes have also been demonstrated.

Rapid assembly of 3-azidomethylfurans from 2-(1-alkynyl)-2-alken-1-ones enabled by silver catalysis

Qian, Lei-Lei,Yi, Ruxia,Min, Xiang-Ting,Hu, Yan-Cheng,Wan, Boshun,Chen, Qing-An

, (2020/06/24)

A rapid access to useful 3-azidomethylfurans is developed via Ag(I)-catalyzed cascade annulation/azidation of 2-(1-alkynyl)-2-alken-1-ones. The salient features of the protocol include mild reaction conditions, high efficiency, broad substrate scope, and

Solvolytic stereoselective debromination of vic-dibromides with HMPA

Khurana,Bansal,Chauhan

, p. 1089 - 1091 (2007/10/03)

A simple and efficient procedure for the debromination of vic-dibromides has been reported with hexamethylphosphoric triamide at 155-160°C under a nitrogen atmosphere without the aid of any reagent.

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