2-(2-Bromophenyl)-1-phenylethanone, with the CAS number 16897-97-5, is an organic compound characterized by its ketone functional group and the presence of bromine and phenyl groups. This compound features a central carbon atom bonded to a phenyl group and a 2-bromophenyl group, which contributes to its unique reactivity and properties. It typically appears as a solid at room temperature and is soluble in organic solvents such as ethanol and acetone, but has limited solubility in water due to its hydrophobic nature. The presence of the bromine atom enhances its electrophilic character, making it useful in various chemical reactions, including electrophilic aromatic substitution. Additionally, this compound may exhibit interesting photophysical properties, making it a candidate for applications in organic synthesis and materials science. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled, and appropriate protective equipment should be used.

2-(2-bromophenyl)-1-phenylethanone

16897-97-5: Ethanone, 2-(2-Bromophenyl)-1-Phenyl-

2-(2-Bromophenyl)acetophenone

2-(2-Bromophenyl)acetophenone is the chemical compound with the formula C8H7BrO. It is a colorless liquid that is soluble in organic solvents. 2-(2-Bromophenyl)acetophenone can be prepared by the reaction of acetophenone with bromine, which yields an enolate anion and a radical anion. This reaction requires irradiation with ultraviolet light or exposure to sunlight. The monosubstituted aromatic ketones are obtained by refluxing 2-(2-bromophenyl)acetophenone in ethanol with sodium ethoxide and acetic acid as a catalyst. Yields of these reactions depend on the reactant concentrations and solvent used.

CAS 16897-97-5: 2-(2-bromophenyl)-1-phenylethanone

2-(2-Bromophenyl)acetophenone

Ref: 10-F203755

2-(2-Bromophenyl)acetophenone

Ref: 3D-RAA89797

Ethanone, 2-(2-bromophenyl)-1-phenyl-

Ref: IN-DA001YFA