2-Nitro-4-(trifluoromethyl)benzamide is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with a nitro group and a trifluoromethyl group. The presence of the nitro group (-NO2) introduces a strong electron-withdrawing effect, influencing the compound's reactivity and polarity. The trifluoromethyl group (-CF3) is another significant substituent that enhances the compound's lipophilicity and stability, making it useful in various chemical applications. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its unique combination of functional groups allows it to participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, due to the presence of both nitro and trifluoromethyl groups, it may exhibit interesting biological activities, making it a subject of interest in pharmaceutical research. Safety precautions should be taken when handling this compound, as it may pose health risks due to its chemical nature.

2-nitro-4-(trifluoromethyl)benzamide

22227-55-0: 2-Nitro-4-(trifluoromethyl)benzamide is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with a nitro group and a trifluoromethyl group. The presence of the nitro group (-NO2) introduces a strong electron-withdrawing effect, influencing the compound's reactivity and polarity. The trifluoromethyl group (-CF3) is another significant substituent that enhances the compound's lipophilicity and stability, making it useful in various chemical applications. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its unique combination of functional groups allows it to participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, due to the presence of both nitro and trifluoromethyl groups, it may exhibit interesting biological activities, making it a subject of interest in pharmaceutical research. Safety precautions should be taken when handling this compound, as it may pose health risks due to its chemical nature.

CAS 22227-55-0

2-nitro-4-(trifluoromethyl)benzamide

2-Nitro-4-trifluoromethylbenzamide

Ref: IN-DA003HS5

2-Nitro-4-(trifluoromethyl)benzamide

Ref: 54-PC7956