4-Nitrobenzamide is an organic compound characterized by the presence of a nitro group (-NO2) and an amide group (-CONH2) attached to a benzene ring. Its molecular formula is C7H6N2O3, indicating it contains seven carbon atoms, six hydrogen atoms, two nitrogen atoms, and three oxygen atoms. This compound typically appears as a yellow crystalline solid and is known for its moderate solubility in polar solvents like water and ethanol. 4-Nitrobenzamide is often utilized in organic synthesis and as an intermediate in the production of dyes, pharmaceuticals, and agrochemicals. The presence of the nitro group contributes to its reactivity, making it a useful building block in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, it exhibits properties that may be of interest in studies related to its biological activity, although specific applications can vary widely depending on the context of its use. Safety precautions should be observed when handling this compound, as it may pose health risks if ingested or inhaled.

4-Nitrobenzamide

619-80-7: 4 Nitro Benzamide, Benzamide, 4-nitro-, Benzamide, p-nitro-, NSC 2902, p-Nitrobenzamide, 4-Nitrobenzamide

4-Nitrobenzamide is a chemical substance that belongs to the class of nitrobenzamides. It is used as an intermediate in the synthesis of other substances, such as pharmaceuticals, herbicides, and pesticides. 4-Nitrobenzamide was first synthesized in 1894 by hydrogenating nitrobenzoic acid with hydrogen chloride in the presence of phosphorus pentachloride. The reaction vessel for this process should be made of glass or porcelain due to the corrosive nature of hydrogen chloride gas. The kinetics for this reaction were studied using concentration-response curves on rats and mice at different concentrations. Acute toxicities observed include respiratory distress and death in rats and convulsions and death in mice.
4-Nitrobenzamide is also toxic to bacteria, which can be seen by its effect on Staphylococcus aureus (strain ATCC 25923). This strain had a 50% survival rate after exposure

CAS 619-80-7: 4-Nitrobenzamide

4-Nitrobenzamide

Ref: 3B-N0323

4-Nitrobenzamide

Ref: 3D-FN02090

4-Nitrobenzamide

Ref: 10-F209414

4-Nitrobenzamide

Ref: 54-OR27669

4-Nitrobenzamide

Ref: 7W-GK9062