2-Fluoro-3-(trifluoromethyl)benzamide is an aromatic compound characterized by the presence of a benzene ring substituted with a fluorine atom and a trifluoromethyl group, along with an amide functional group. The molecular structure features a fluorine atom at the second position and a trifluoromethyl group at the third position of the benzene ring, which significantly influences its chemical properties. This compound is typically a solid at room temperature and exhibits moderate solubility in organic solvents. The presence of the trifluoromethyl group enhances its lipophilicity and can affect its reactivity, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. The amide functional group contributes to its potential as a hydrogen bond donor and acceptor, influencing its interactions in biological systems. Overall, 2-fluoro-3-(trifluoromethyl)benzamide is notable for its unique combination of fluorinated substituents, which can impart distinct physical and chemical properties compared to non-fluorinated analogs.

2-fluoro-3-(trifluoromethyl)benzamide

207919-05-9: 2-Fluoro-3-(trifluoromethyl)benzamide is an aromatic compound characterized by the presence of a benzene ring substituted with a fluorine atom and a trifluoromethyl group, along with an amide functional group. The molecular structure features a fluorine atom at the second position and a trifluoromethyl group at the third position of the benzene ring, which significantly influences its chemical properties. This compound is typically a solid at room temperature and exhibits moderate solubility in organic solvents. The presence of the trifluoromethyl group enhances its lipophilicity and can affect its reactivity, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. The amide functional group contributes to its potential as a hydrogen bond donor and acceptor, influencing its interactions in biological systems. Overall, 2-fluoro-3-(trifluoromethyl)benzamide is notable for its unique combination of fluorinated substituents, which can impart distinct physical and chemical properties compared to non-fluorinated analogs.

CAS 207919-05-9

2-fluoro-3-(trifluoromethyl)benzamide

Benzamide, 2-fluoro-5-(trifluoromethyl)-

Ref: IN-DA002JDL

2-Fluoro-5-(trifluoromethyl)benzamide

Ref: 54-PC4371T

2-Fluoro-5-(trifluoromethyl)benzamide

Ref: 10-F006389