1-(4-Fluorophenyl)-3-phenylprop-2-en-1-one, also known as 4-Fluorobenzylideneacetophenone, is an organic compound characterized by its structure, which features a conjugated system comprising a fluorinated phenyl group and a phenylprop-2-en-1-one moiety. This compound typically appears as a yellow to orange solid and is known for its potential applications in organic synthesis and as a building block in the development of pharmaceuticals and agrochemicals. It exhibits properties such as moderate solubility in organic solvents and may show fluorescence under UV light. The presence of the fluorine atom can influence its reactivity and electronic properties, making it a subject of interest in medicinal chemistry. Additionally, it may undergo various chemical reactions, including electrophilic substitutions and Michael additions, due to the presence of the α,β-unsaturated carbonyl group. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled.

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

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4'-Fluorochalcone

4'-Fluorochalcone is a mutagenic molecule that belongs to the group of chalcones. It has been shown to be thermodynamically stable and can be labeled with magnetic particles. 4'-Fluorochalcone is a conformationally restricted molecule and has been found to have mutagenic properties in centroid, dihedral, and covid-19 pandemic parameters. This molecule is also a mutagen in the sense that it induces mutations on DNA by binding to DNA bases at specific sites and causing a change in their shapes. The shape of these bases changes, which results in an alteration of the gene sequence.

CAS 399-10-0: 1-(4-fluorophenyl)-3-phenylprop-2-en-1-one

4'-Fluorochalcone

Ref: 3B-F0425

4'-Fluorochalcone

Ref: 3D-FF53879

4'-Fluorochalcone

Ref: 54-PC3942

4'-FLUOROCHALCONE

Ref: IN-DA003LFC

4'-Fluorochalcone

Ref: 10-F005222