2-[(4-Chlorophenyl)sulfanyl]-5-nitrobenzaldehyde is an organic compound characterized by its complex structure, which includes a nitro group, a chlorophenyl group, and a sulfanyl group attached to a benzaldehyde framework. The presence of the nitro group (-NO2) typically imparts significant electron-withdrawing properties, influencing the compound's reactivity and polarity. The chlorophenyl moiety contributes to the compound's hydrophobic characteristics and can affect its biological activity. The sulfanyl group (-S-) introduces a sulfur atom, which can participate in various chemical reactions, including nucleophilic substitutions and redox reactions. This compound is likely to be a yellow to brown solid at room temperature, exhibiting moderate solubility in organic solvents. Its unique functional groups suggest potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. Additionally, the compound's properties may be influenced by factors such as pH, solvent choice, and temperature, which can affect its stability and reactivity in different environments.

2-[(4-chlorophenyl)sulfanyl]-5-nitrobenzaldehyde

42191-01-5: 2-[(4-Chlorophenyl)sulfanyl]-5-nitrobenzaldehyde is an organic compound characterized by its complex structure, which includes a nitro group, a chlorophenyl group, and a sulfanyl group attached to a benzaldehyde framework. The presence of the nitro group (-NO2) typically imparts significant electron-withdrawing properties, influencing the compound's reactivity and polarity. The chlorophenyl moiety contributes to the compound's hydrophobic characteristics and can affect its biological activity. The sulfanyl group (-S-) introduces a sulfur atom, which can participate in various chemical reactions, including nucleophilic substitutions and redox reactions. This compound is likely to be a yellow to brown solid at room temperature, exhibiting moderate solubility in organic solvents. Its unique functional groups suggest potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. Additionally, the compound's properties may be influenced by factors such as pH, solvent choice, and temperature, which can affect its stability and reactivity in different environments.

CAS 42191-01-5

2-[(4-chlorophenyl)sulfanyl]-5-nitrobenzaldehyde

2-((4-Chlorophenyl)thio)-5-nitrobenzaldehyde

Ref: IN-DA00CJCR

5-Nitro-2-(4-chlorophenylthio)benzaldehyde

Ref: 54-OR13138