3-(3-Bromophenyl)cyclobutanone is an organic compound characterized by its cyclobutanone structure, which features a four-membered carbon ring with a ketone functional group. The presence of a bromophenyl group at the 3-position of the cyclobutanone ring introduces significant steric and electronic effects, influencing its reactivity and properties. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the bromine substituent, which can enhance biological activity or modulate interactions with biological targets. The compound's reactivity may include typical ketone reactions, such as nucleophilic addition and condensation, making it a versatile intermediate in organic synthesis. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 3-(3-Bromophenyl)cyclobutanone is a noteworthy compound in the realm of organic chemistry, with implications for further research and application in various chemical fields.

3-(3-Bromophenyl)cyclobutanone

885267-15-2: Cyclobutanone, 3-(3-Bromophenyl)-

3-(3-Bromophenyl)-cyclobutanone is a chemical compound with the molecular formula of C8H6BrO. It is a peroxide that is synthesized by the lactonization of cyclobutanone with 3-bromophenol in the presence of an oxidizing agent such as potassium permanganate or hydrogen peroxide. The family of compounds that are synthesized using this reaction includes ketones, cyclobutanones, and oximes. The synthesis can be optimized by varying the substrate concentration and reaction time. This product has been used to synthesize lipase substrates with high yields and chemoenzymatic oxidation products.

CAS 885267-15-2: 3-(3-Bromophenyl)cyclobutanone

3-(3-Bromophenyl)-cyclobutanone

Ref: 3D-FB150236

3-(3-Bromophenyl)cyclobutanone

Ref: IN-DA0089Q9

3-(3-Bromophenyl)cyclobutan-1-one

Ref: 10-F603214