4-Bromochalcone is an organic compound belonging to the chalcone class, characterized by its structure that features a phenyl group and an α,β-unsaturated carbonyl system. It is typically represented by the formula C15H12BrO, indicating the presence of a bromine atom, which contributes to its unique chemical properties. This compound is known for its yellow crystalline appearance and is often utilized in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. 4-Bromochalcone exhibits notable biological activities, including potential anti-inflammatory and antimicrobial properties, making it a subject of interest in medicinal chemistry. Its reactivity is influenced by the presence of the bromine substituent, which can participate in electrophilic aromatic substitution reactions. Additionally, 4-Bromochalcone can undergo various transformations, such as reduction or cyclization, to yield diverse derivatives with potentially enhanced biological activities. As with many organic compounds, proper handling and safety precautions are essential due to its chemical nature and potential toxicity.

4-Bromochalcone

1774-66-9: (2E)-3-(4-Bromophenyl)-1-phenyl-2-propen-1-one, 1-Phenyl-3-(4-bromophenyl)-2-propen-1-one, 2-Propen-1-one, 3- (4-bromophenyl)-1-phenyl-, 2-Propen-1-one, 3-(4-bromophenyl)-1-phenyl-, (E)-, 2-propen-1-one, 3-(4-bromophenyl)-1-phenyl-, (2E)-, 3-(4-Bromophenyl)-1-phenyl-2-propen-1-one, 3-(4-Bromophenyl)-1-phenyl-2-propene-1-one, 3-(4-Bromophenyl)-1-phenyl-2-propenone, 4-Bromochalcone, 4-Bromostyryl phenyl ketone, Chalcone, 4-bromo-, NSC 28482, NSC 636922, p-Bromochalcone, p-Bromostyryl phenyl ketone, trans-4-Bromochalcone

2-Propen-1-one, 3-(4-bromophenyl)-1-phenyl-

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

3-(4-Bromophenyl)-1-phenyl-2-propen-1-one is a synthetic compound that acts as a potent inducer of enzymes that metabolize xenobiotics. It has been shown to have an inhibitory effect on the liver enzyme 3-methylcholanthrene, which is involved in the metabolism of carcinogenic hydrocarbons such as benzopyrene. This compound also inhibits cholesterol synthesis and can be used as a dietary supplement in humans. The functional group of 3-(4-bromophenyl)-1-phenyl-2-propen-1-one is a dipole, which gives it its reactivity. The molecule can be synthesized from acetophenone and bromine.

CAS 1774-66-9: 4-Bromochalcone

2-Propen-1-one, 3-(4-bromophenyl)-1-phenyl-

Ref: IN-DA0025AQ

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

Ref: 3B-B6397

4-Bromochalcone

Ref: 54-OR27797

3-(4-Bromophenyl)-1-phenyl-2-propen-1-one

Ref: 3D-BAA77466