3-Fluoro-N-phenylaniline, with the CAS number 500-41-4, is an organic compound characterized by the presence of a fluorine atom attached to the aromatic ring of phenylaniline. This compound features an aniline structure, where an amino group (-NH2) is directly bonded to a phenyl group, and the fluorine substituent is located at the meta position relative to the amino group. The presence of the fluorine atom can influence the compound's physical and chemical properties, such as its reactivity, solubility, and boiling point. Typically, compounds like 3-fluoro-N-phenylaniline are used in various applications, including as intermediates in the synthesis of pharmaceuticals, agrochemicals, and dyes. The compound may exhibit moderate toxicity, and safety precautions should be taken when handling it. Its molecular structure contributes to its potential as a building block in organic synthesis, particularly in the development of more complex molecules. As with many fluorinated compounds, it may also display unique electronic properties due to the electronegative nature of fluorine.

3-fluoro-N-phenylaniline

500-41-4: 3-Fluoro-N-phenylaniline, with the CAS number 500-41-4, is an organic compound characterized by the presence of a fluorine atom attached to the aromatic ring of phenylaniline. This compound features an aniline structure, where an amino group (-NH2) is directly bonded to a phenyl group, and the fluorine substituent is located at the meta position relative to the amino group. The presence of the fluorine atom can influence the compound's physical and chemical properties, such as its reactivity, solubility, and boiling point. Typically, compounds like 3-fluoro-N-phenylaniline are used in various applications, including as intermediates in the synthesis of pharmaceuticals, agrochemicals, and dyes. The compound may exhibit moderate toxicity, and safety precautions should be taken when handling it. Its molecular structure contributes to its potential as a building block in organic synthesis, particularly in the development of more complex molecules. As with many fluorinated compounds, it may also display unique electronic properties due to the electronegative nature of fluorine.

CAS 500-41-4

3-fluoro-N-phenylaniline

3-Fluorodiphenylamine

Ref: 54-PC2799

3-FLUORODIPHENYLAMINE

Ref: 10-F330827