4-Amino-3-nitro-acetophenone, with the CAS number 1432-42-4, is an organic compound characterized by the presence of an acetophenone structure substituted with both an amino group and a nitro group. This compound typically appears as a solid, often in a crystalline form, and is known for its yellowish color. It is soluble in organic solvents such as ethanol and acetone but has limited solubility in water. The presence of the amino group (-NH2) contributes to its basicity, while the nitro group (-NO2) is known for its electron-withdrawing properties, influencing the compound's reactivity and stability. 4-Amino-3-nitro-acetophenone is often used in organic synthesis and may serve as an intermediate in the production of dyes, pharmaceuticals, and other chemical compounds. Its reactivity can be attributed to the functional groups present, allowing for various chemical transformations. As with many nitro compounds, it may pose certain hazards, necessitating careful handling and storage.

4-AMINO-3-NITRO-ACETOPHENONE

1432-42-4: 1-(4-Amino-3-nitrophenyl)ethanone, Ethanone, 1-(4-Amino-3-Nitrophenyl)-

1-(4-Amino-3-nitrophenyl)ethan-1-one

4-Amino-3-nitroacetophenone is a ketone that is synthesized by the reaction of acetophenone and nitric acid. It has been used as a precursor in the production of dyes, pharmaceuticals, and explosives. The conversion of 4-amino-3-nitroacetophenone to 2,4,6-trinitrophenol is catalyzed by aluminium powder or activated charcoal. This reagent converts the amide group to an amine group by reacting with water in the presence of oxygen. Diethyl ether can be used as a solvent for this reaction.

CAS 1432-42-4: 4-AMINO-3-NITRO-ACETOPHENONE

4-AMINO-3-NITRO-ACETOPHENONE

Ref: IN-DA009BHJ

1-(4-Amino-3-nitrophenyl)ethan-1-one

Ref: 54-OR75842

1-(4-Amino-3-nitrophenyl)ethan-1-one

Ref: 10-F639629

4-Amino-3-nitroacetophenone

Ref: 3D-FA11486