3-Bromo-4-iodoacetophenone is an organic compound characterized by the presence of both bromine and iodine substituents on the aromatic ring of an acetophenone structure. It features a ketone functional group, which contributes to its reactivity and potential applications in organic synthesis. The compound typically appears as a solid at room temperature and is soluble in organic solvents such as dichloromethane and acetone, but may have limited solubility in water due to its hydrophobic aromatic nature. The presence of halogens (bromine and iodine) enhances its electrophilic properties, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the compound may exhibit interesting biological activities, which can be explored in medicinal chemistry. Safety precautions should be taken when handling this compound, as halogenated compounds can be hazardous. Overall, 3-Bromo-4-iodoacetophenone serves as a valuable intermediate in the synthesis of more complex organic molecules.

3-Bromo-4-iodoacetophenone

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CAS 945907-32-4: 3-Bromo-4-iodoacetophenone

1-(3-Bromo-4-iodophenyl)ethanone

Ref: IN-DA00IID6

3'-Bromo-4'-iodoacetophenone

Ref: 3D-VMB90732

3'-Bromo-4'-iodoacetophenone

Ref: 54-OR400426

1-(3-Bromo-4-iodophenyl)ethanone

Ref: 10-F519699