(3,4-Dichlorophenyl)(4-fluorophenyl)methanone, with the CAS number 157428-51-8, is an organic compound characterized by its aromatic structure and the presence of multiple halogen substituents. This compound features a ketone functional group, which is indicated by the "methanone" part of its name, and it consists of two phenyl rings: one substituted with two chlorine atoms at the 3 and 4 positions and the other with a fluorine atom at the para position. The presence of these halogens can significantly influence the compound's chemical reactivity, stability, and potential biological activity. Generally, compounds with such substituents may exhibit interesting properties, including altered solubility and potential applications in pharmaceuticals or agrochemicals. The molecular structure suggests that it may participate in various chemical reactions, including electrophilic aromatic substitution, due to the electron-withdrawing nature of the halogens. Additionally, the compound's physical properties, such as melting point and boiling point, would be influenced by the presence of these substituents, affecting its behavior in different environments.

(3,4-dichlorophenyl)(4-fluorophenyl)methanone

157428-51-8: (3,4-Dichlorophenyl)(4-fluorophenyl)methanone, with the CAS number 157428-51-8, is an organic compound characterized by its aromatic structure and the presence of multiple halogen substituents. This compound features a ketone functional group, which is indicated by the "methanone" part of its name, and it consists of two phenyl rings: one substituted with two chlorine atoms at the 3 and 4 positions and the other with a fluorine atom at the para position. The presence of these halogens can significantly influence the compound's chemical reactivity, stability, and potential biological activity. Generally, compounds with such substituents may exhibit interesting properties, including altered solubility and potential applications in pharmaceuticals or agrochemicals. The molecular structure suggests that it may participate in various chemical reactions, including electrophilic aromatic substitution, due to the electron-withdrawing nature of the halogens. Additionally, the compound's physical properties, such as melting point and boiling point, would be influenced by the presence of these substituents, affecting its behavior in different environments.

CAS 157428-51-8

(3,4-dichlorophenyl)(4-fluorophenyl)methanone

3,4-Dichloro-4'-fluorobenzophenone

Ref: IN-DA001PGK

3,4-Dichloro-4′-fluorobenzophenone

Ref: 10-F202117