3-Ethyl-4-fluorobenzamide is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with an ethyl group and a fluorine atom, along with an amide functional group. The presence of the ethyl group at the meta position and the fluorine atom at the para position relative to the amide group influences its chemical properties, such as polarity and reactivity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents due to its hydrophobic aromatic nature. The fluorine atom can enhance the compound's stability and influence its biological activity, making it of interest in pharmaceutical research. Additionally, the amide functional group contributes to hydrogen bonding capabilities, which can affect its interactions in various chemical environments. Overall, 3-ethyl-4-fluorobenzamide is a compound of interest in synthetic organic chemistry and medicinal chemistry, with potential applications in drug development and material science.

3-ethyl-4-fluorobenzamide

1112179-03-9: 3-Ethyl-4-fluorobenzamide is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with an ethyl group and a fluorine atom, along with an amide functional group. The presence of the ethyl group at the meta position and the fluorine atom at the para position relative to the amide group influences its chemical properties, such as polarity and reactivity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents due to its hydrophobic aromatic nature. The fluorine atom can enhance the compound's stability and influence its biological activity, making it of interest in pharmaceutical research. Additionally, the amide functional group contributes to hydrogen bonding capabilities, which can affect its interactions in various chemical environments. Overall, 3-ethyl-4-fluorobenzamide is a compound of interest in synthetic organic chemistry and medicinal chemistry, with potential applications in drug development and material science.

CAS 1112179-03-9

3-ethyl-4-fluorobenzamide