The chemical substance known as (2E)-1-(4-bromophenyl)-3-phenylprop-2-en-1-one, with the CAS number 22966-23-0, is an organic compound characterized by its conjugated double bond system and the presence of a bromine substituent on the aromatic ring. This compound features a phenyl group and a 4-bromophenyl group attached to a prop-2-en-1-one backbone, which contributes to its reactivity and potential applications in organic synthesis. The presence of the bromine atom enhances its electrophilic properties, making it a useful intermediate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The compound is likely to exhibit properties typical of α,β-unsaturated carbonyl compounds, such as the ability to undergo Michael additions. Its structural features suggest potential applications in pharmaceuticals, agrochemicals, and materials science. Additionally, the compound's stability and solubility characteristics would depend on the solvent and conditions used, which are important for its practical applications in research and industry.

(2E)-1-(4-bromophenyl)-3-phenylprop-2-en-1-one

22966-23-0: (2E)-1-(4-Bromophenyl)-3-phenyl-2-propen-1-one, (E)-1-(4-Bromophenyl)-3-phenyl-2-propen-1-one, 2-Propen-1-one, 1- (4-bromophenyl)-3-phenyl-, 2-propen-1-one, 1-(4-bromophenyl)-3-phenyl-, (2E)-, 2-Propen-1-one, 1-(4-bromophenyl)-3-phenyl-, (E)-, Chalcone, 4'-bromo-, trans-4'-Bromochalcone

CAS 22966-23-0: (2E)-1-(4-bromophenyl)-3-phenylprop-2-en-1-one

trans-4'-Bromochalcone

Ref: 54-OR27786

(2E)-1-(4-bromophenyl)-3-phenylprop-2-en-1-one

Ref: 10-F358337