Benzamide, 4-amino-3-nitro- is an organic compound characterized by the presence of an amide functional group attached to a benzene ring, which also features an amino group and a nitro group at specific positions on the aromatic ring. The compound has a molecular structure that includes a benzene ring substituted with an amino group (-NH2) at the para position and a nitro group (-NO2) at the meta position relative to the amide group. This arrangement contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of both electron-donating (amino) and electron-withdrawing (nitro) groups influences its electronic properties, making it a subject of interest in synthetic organic chemistry. Additionally, the compound may exhibit specific solubility characteristics in polar and non-polar solvents, and its stability can be affected by environmental conditions such as pH and temperature. As with many nitro-substituted compounds, it may also possess biological activity, warranting further investigation into its potential uses.

Benzamide, 4-amino-3-nitro-

41263-65-4: Benzamide, 4-amino-3-nitro- is an organic compound characterized by the presence of an amide functional group attached to a benzene ring, which also features an amino group and a nitro group at specific positions on the aromatic ring. The compound has a molecular structure that includes a benzene ring substituted with an amino group (-NH2) at the para position and a nitro group (-NO2) at the meta position relative to the amide group. This arrangement contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of both electron-donating (amino) and electron-withdrawing (nitro) groups influences its electronic properties, making it a subject of interest in synthetic organic chemistry. Additionally, the compound may exhibit specific solubility characteristics in polar and non-polar solvents, and its stability can be affected by environmental conditions such as pH and temperature. As with many nitro-substituted compounds, it may also possess biological activity, warranting further investigation into its potential uses.

CAS 41263-65-4

Benzamide, 4-amino-3-nitro-

4-Amino-3-nitrobenzamide

Ref: 10-F638329

4-amino-3-nitrobenzamide

Ref: 3D-RBA26365