4-Chloro-N-(3-hydroxyphenyl)-3-nitrobenzamide is an organic compound characterized by its complex structure, which includes a chloro group, a nitro group, and an amide functional group. The presence of the chloro substituent indicates that it is a chlorinated aromatic compound, while the nitro group contributes to its potential reactivity and polarity. The hydroxyl group on the phenyl ring enhances its solubility in polar solvents and may also influence its biological activity. This compound is likely to exhibit properties typical of nitrobenzamides, such as potential antibacterial or anticancer activity, making it of interest in pharmaceutical research. Its molecular structure suggests that it may participate in hydrogen bonding due to the hydroxyl and amide functionalities, which can affect its interactions with biological targets. Additionally, the presence of multiple functional groups may lead to varied reactivity under different conditions, making it a versatile compound in synthetic organic chemistry. As with many such compounds, safety and handling precautions should be observed due to potential toxicity associated with the nitro and chloro groups.

4-chloro-N-(3-hydroxyphenyl)-3-nitrobenzamide

416887-71-3: 4-Chloro-N-(3-hydroxyphenyl)-3-nitrobenzamide is an organic compound characterized by its complex structure, which includes a chloro group, a nitro group, and an amide functional group. The presence of the chloro substituent indicates that it is a chlorinated aromatic compound, while the nitro group contributes to its potential reactivity and polarity. The hydroxyl group on the phenyl ring enhances its solubility in polar solvents and may also influence its biological activity. This compound is likely to exhibit properties typical of nitrobenzamides, such as potential antibacterial or anticancer activity, making it of interest in pharmaceutical research. Its molecular structure suggests that it may participate in hydrogen bonding due to the hydroxyl and amide functionalities, which can affect its interactions with biological targets. Additionally, the presence of multiple functional groups may lead to varied reactivity under different conditions, making it a versatile compound in synthetic organic chemistry. As with many such compounds, safety and handling precautions should be observed due to potential toxicity associated with the nitro and chloro groups.

CAS 416887-71-3

4-chloro-N-(3-hydroxyphenyl)-3-nitrobenzamide

4-Chloro-n-(3-hydroxyphenyl)-3-nitrobenzamide

Ref: IN-DA00C5YO

4-chloro-N-(3-hydroxyphenyl)-3-nitrobenzamide

Ref: 10-F314150