The chemical substance known as (2E)-3-(4-bromophenyl)-1-phenylprop-2-en-1-one, with the CAS number 22966-09-2, is an organic compound characterized by its conjugated double bond system and the presence of a bromine atom on the phenyl ring. This compound features a chalcone structure, which is typically known for its role in various biological activities, including anti-inflammatory and antioxidant properties. The presence of the bromine substituent enhances its reactivity and may influence its biological interactions. The compound is likely to exhibit a yellow to orange color, typical of many chalcones, and is soluble in organic solvents. Its molecular structure allows for potential applications in organic synthesis and as a precursor in the development of pharmaceuticals. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the bromine atom and the phenyl groups, making it a subject of interest in both synthetic and medicinal chemistry.

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

22966-09-2: (2E)-3-(4-Bromophenyl)-1-phenyl-2-propen-1-one, 2-Propen-1-one, 3- (4-bromophenyl)-1-phenyl-, 2-propen-1-one, 3-(4-bromophenyl)-1-phenyl-, (2E)-, 2-Propen-1-one, 3-(4-bromophenyl)-1-phenyl-, (E)-, trans-4-Bromochalcone

4'-Bromochalcone is a chalcone derivative that is used as a synthetic intermediate. It can be prepared by the cross-coupling of disulfides and epoxides with radical mechanism in an efficient method. The product can be obtained from β-unsaturated ketones, such as acetonitrile, indian, chloride, and sodium sulfide. 4'-Bromochalcone has cytotoxic effects on cancer cell lines. In addition, it has been reported to inhibit the proliferation of rat hepatoma cells and human breast cancer cells in vitro.

CAS 22966-09-2: (2E)-3-(4-bromophenyl)-1-phenylprop-2-en-1-one

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

Ref: 10-F524273

4'-Bromochalcone

Ref: 3D-FB53878

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

Ref: IN-DA00BPMS