3,5-Difluoro-4-nitroaniline is an organic compound characterized by the presence of two fluorine atoms and a nitro group attached to an aniline structure. Its molecular formula typically includes carbon, hydrogen, nitrogen, and fluorine, reflecting its aromatic nature. The compound is a derivative of aniline, where the amino group (-NH2) is substituted with a nitro group (-NO2) and two fluorine atoms at the 3 and 5 positions on the benzene ring. This substitution pattern can influence its chemical reactivity, solubility, and potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of the nitro group generally enhances the compound's electron-withdrawing properties, which can affect its acidity and reactivity in electrophilic aromatic substitution reactions. Additionally, the fluorine atoms can impart unique properties such as increased lipophilicity and altered biological activity. Safety data sheets should be consulted for handling and toxicity information, as compounds with nitro and fluorine substituents can pose health and environmental risks.

3,5-DIFLUORO-4-NITROANILINE

122129-79-7: 3,5-Difluoro-4-nitroaniline is an organic compound characterized by the presence of two fluorine atoms and a nitro group attached to an aniline structure. Its molecular formula typically includes carbon, hydrogen, nitrogen, and fluorine, reflecting its aromatic nature. The compound is a derivative of aniline, where the amino group (-NH2) is substituted with a nitro group (-NO2) and two fluorine atoms at the 3 and 5 positions on the benzene ring. This substitution pattern can influence its chemical reactivity, solubility, and potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of the nitro group generally enhances the compound's electron-withdrawing properties, which can affect its acidity and reactivity in electrophilic aromatic substitution reactions. Additionally, the fluorine atoms can impart unique properties such as increased lipophilicity and altered biological activity. Safety data sheets should be consulted for handling and toxicity information, as compounds with nitro and fluorine substituents can pose health and environmental risks.

CAS 122129-79-7

3,5-DIFLUORO-4-NITROANILINE

Benzenamine, 3,5-difluoro-4-nitro-

Ref: IN-DA0016TM

3,5-Difluoro-4-nitroaniline

Ref: 54-PC5188

3,5-Difluoro-4-nitroaniline

Ref: 10-F221537