2-Bromo-N-(2,4-difluorophenyl)benzamide is an organic compound characterized by its structural features, which include a benzamide moiety substituted with a bromine atom and a difluorophenyl group. The presence of the bromine atom introduces notable reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The difluorophenyl group enhances the compound's lipophilicity and may influence its biological activity, as fluorine atoms can significantly alter the electronic properties of the molecule. This compound is likely to exhibit moderate to high stability under standard conditions, but its reactivity can be influenced by the presence of functional groups and the overall molecular structure. It may be soluble in organic solvents, while its solubility in water could be limited due to the hydrophobic nature of the aromatic rings. Additionally, 2-bromo-N-(2,4-difluorophenyl)benzamide may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its unique structural characteristics that can interact with biological targets.

2-bromo-N-(2,4-difluorophenyl)benzamide

314025-94-0: 2-Bromo-N-(2,4-difluorophenyl)benzamide is an organic compound characterized by its structural features, which include a benzamide moiety substituted with a bromine atom and a difluorophenyl group. The presence of the bromine atom introduces notable reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The difluorophenyl group enhances the compound's lipophilicity and may influence its biological activity, as fluorine atoms can significantly alter the electronic properties of the molecule. This compound is likely to exhibit moderate to high stability under standard conditions, but its reactivity can be influenced by the presence of functional groups and the overall molecular structure. It may be soluble in organic solvents, while its solubility in water could be limited due to the hydrophobic nature of the aromatic rings. Additionally, 2-bromo-N-(2,4-difluorophenyl)benzamide may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its unique structural characteristics that can interact with biological targets.

CAS 314025-94-0

2-bromo-N-(2,4-difluorophenyl)benzamide

N-(2,4-Difluorophenyl) 2-bromobenzamide

Ref: IN-DA003S7V

2-Bromo-N-(2,4-difluorophenyl)benzamide

Ref: 54-PC7146