2-(Difluoromethoxy)-4-fluoroaniline is an organic compound characterized by its unique molecular structure, which includes an aniline group substituted with both a difluoromethoxy and a fluoro group. This compound typically exhibits properties associated with aromatic amines, such as moderate solubility in polar solvents and potential reactivity due to the presence of the amino group. The difluoromethoxy substituent introduces significant electronegativity, influencing the compound's electronic properties and reactivity. The presence of multiple fluorine atoms enhances its lipophilicity and may affect its biological activity, making it of interest in pharmaceutical research. Additionally, the compound's stability can be influenced by the steric and electronic effects of the substituents. Safety considerations should be taken into account, as fluorinated compounds can exhibit unique toxicological profiles. Overall, 2-(difluoromethoxy)-4-fluoroaniline represents a class of compounds that may have applications in medicinal chemistry and materials science due to their distinctive chemical characteristics.

2-(difluoromethoxy)-4-fluoroaniline

832740-98-4: 2-(Difluoromethoxy)-4-fluoroaniline is an organic compound characterized by its unique molecular structure, which includes an aniline group substituted with both a difluoromethoxy and a fluoro group. This compound typically exhibits properties associated with aromatic amines, such as moderate solubility in polar solvents and potential reactivity due to the presence of the amino group. The difluoromethoxy substituent introduces significant electronegativity, influencing the compound's electronic properties and reactivity. The presence of multiple fluorine atoms enhances its lipophilicity and may affect its biological activity, making it of interest in pharmaceutical research. Additionally, the compound's stability can be influenced by the steric and electronic effects of the substituents. Safety considerations should be taken into account, as fluorinated compounds can exhibit unique toxicological profiles. Overall, 2-(difluoromethoxy)-4-fluoroaniline represents a class of compounds that may have applications in medicinal chemistry and materials science due to their distinctive chemical characteristics.

CAS 832740-98-4

2-(difluoromethoxy)-4-fluoroaniline

2-(Difluoromethoxy)-4-fluoroaniline

Ref: 54-PC501980

2-Difluoromethoxy-4-fluoro-phenylamine

Ref: 3D-HIB74098