2,6-Difluoro-3-nitrobenzenamine, with the CAS number 25892-09-5, is an organic compound characterized by the presence of both fluorine and nitro functional groups attached to a benzene ring. This compound features two fluorine atoms located at the 2 and 6 positions of the aromatic ring, while a nitro group is positioned at the 3 position, along with an amino group (-NH2) at the 1 position. The presence of these substituents influences its chemical reactivity and physical properties, such as solubility and boiling point. Typically, compounds like this exhibit moderate polarity due to the electronegative fluorine and nitro groups, which can also enhance their reactivity in electrophilic aromatic substitution reactions. Additionally, the amino group can participate in hydrogen bonding, affecting the compound's interactions in various environments. Overall, 2,6-Difluoro-3-nitrobenzenamine is of interest in fields such as pharmaceuticals and agrochemicals, where its unique structure may contribute to specific biological activities or chemical properties.

2,6-Difluoro-3-nitrobenzenamine

25892-09-5: 2,6-Difluoro-3-nitrobenzenamine, 2,6-Difluoro-5-nitroaniline, Aniline, 2,6-difluoro-3-nitro-, Benzenamine, 2,6-difluoro-3-nitro-, Zr Bf Ff Cnw, 2,6-Difluoro-3-nitroaniline

2,6-difluoro-3-nitroaniline

2,6-Difluoro-3-nitroaniline

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CAS 25892-09-5: 2,6-Difluoro-3-nitrobenzenamine

2,6-difluoro-3-nitroaniline

Ref: IN-DA00C3V7

2,6-Difluoro-3-nitroaniline

Ref: 10-F209634

2,6-difluoro-3-nitroaniline

Ref: 3D-FD104913

2,6-Difluoro-3-nitroaniline

Ref: 54-PC57022