Benzenamine, tetrafluoro- (CAS 71964-99-3), also known as tetrafluorobenzenamine, is an aromatic amine characterized by the presence of a benzene ring substituted with four fluorine atoms and an amino group (-NH2). This compound exhibits a high degree of fluorination, which significantly influences its chemical properties, including increased electronegativity and altered reactivity compared to non-fluorinated analogs. The presence of fluorine atoms enhances the compound's stability and lipophilicity, making it less reactive towards nucleophiles. Benzenamine, tetrafluoro- is typically a colorless to pale yellow solid at room temperature and is soluble in organic solvents. Its applications may include use in the synthesis of specialty chemicals, pharmaceuticals, and agrochemicals, where fluorinated compounds are often sought for their unique properties. However, due to the potential environmental and health impacts of fluorinated compounds, handling and disposal must be conducted with care, adhering to safety regulations.

Benzenamine, tetrafluoro-

71964-99-3: Benzenamine, tetrafluoro- (CAS 71964-99-3), also known as tetrafluorobenzenamine, is an aromatic amine characterized by the presence of a benzene ring substituted with four fluorine atoms and an amino group (-NH2). This compound exhibits a high degree of fluorination, which significantly influences its chemical properties, including increased electronegativity and altered reactivity compared to non-fluorinated analogs. The presence of fluorine atoms enhances the compound's stability and lipophilicity, making it less reactive towards nucleophiles. Benzenamine, tetrafluoro- is typically a colorless to pale yellow solid at room temperature and is soluble in organic solvents. Its applications may include use in the synthesis of specialty chemicals, pharmaceuticals, and agrochemicals, where fluorinated compounds are often sought for their unique properties. However, due to the potential environmental and health impacts of fluorinated compounds, handling and disposal must be conducted with care, adhering to safety regulations.