2-(2-Fluorophenyl)-1-(4-iodophenyl)ethanone, with the CAS number 187617-12-5, is an organic compound characterized by its ketone functional group and the presence of both fluorine and iodine substituents on its aromatic rings. This compound features a two-phenyl structure, where one phenyl group is substituted with a fluorine atom at the ortho position, and the other phenyl group has an iodine atom at the para position. The presence of these halogens can significantly influence the compound's reactivity, stability, and solubility. Generally, compounds like this may exhibit interesting biological activities, making them potential candidates for pharmaceutical applications. Additionally, the molecular structure suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, due to the electron-withdrawing effects of the halogens. Its physical properties, such as melting point, boiling point, and solubility, would typically be determined through experimental methods, as they can vary based on the specific conditions and purity of the sample.

2-(2-fluorophenyl)-1-(4-iodophenyl)ethanone

187617-12-5: 2-(2-Fluorophenyl)-1-(4-iodophenyl)ethanone, with the CAS number 187617-12-5, is an organic compound characterized by its ketone functional group and the presence of both fluorine and iodine substituents on its aromatic rings. This compound features a two-phenyl structure, where one phenyl group is substituted with a fluorine atom at the ortho position, and the other phenyl group has an iodine atom at the para position. The presence of these halogens can significantly influence the compound's reactivity, stability, and solubility. Generally, compounds like this may exhibit interesting biological activities, making them potential candidates for pharmaceutical applications. Additionally, the molecular structure suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, due to the electron-withdrawing effects of the halogens. Its physical properties, such as melting point, boiling point, and solubility, would typically be determined through experimental methods, as they can vary based on the specific conditions and purity of the sample.

CAS 187617-12-5

2-(2-fluorophenyl)-1-(4-iodophenyl)ethanone

2-(2-fluorophenyl)-4′-iodoacetophenone

Ref: 10-F203827