5-Chloro-1-(3-nitrophenyl)pentan-1-one is an organic compound characterized by its structural features, which include a pentanone backbone with a chlorine atom and a nitrophenyl group. The presence of the chlorine atom introduces a halogen functionality, which can influence the compound's reactivity and polarity. The nitrophenyl group, containing a nitro functional group (-NO2) attached to a phenyl ring, contributes to the compound's potential for electrophilic substitution reactions and can enhance its electron-withdrawing properties. This compound is likely to exhibit moderate solubility in organic solvents due to its hydrophobic alkyl chain and polar functional groups. Its molecular structure suggests potential applications in pharmaceuticals or as an intermediate in organic synthesis, particularly in the development of biologically active compounds. Additionally, the presence of both a ketone and nitro group may impart unique chemical properties, such as increased acidity or reactivity under certain conditions. Safety and handling precautions should be observed, as with many halogenated and nitro compounds, due to potential toxicity and environmental concerns.

5-chloro-1-(3-nitrophenyl)pentan-1-one

487058-74-2: 5-Chloro-1-(3-nitrophenyl)pentan-1-one is an organic compound characterized by its structural features, which include a pentanone backbone with a chlorine atom and a nitrophenyl group. The presence of the chlorine atom introduces a halogen functionality, which can influence the compound's reactivity and polarity. The nitrophenyl group, containing a nitro functional group (-NO2) attached to a phenyl ring, contributes to the compound's potential for electrophilic substitution reactions and can enhance its electron-withdrawing properties. This compound is likely to exhibit moderate solubility in organic solvents due to its hydrophobic alkyl chain and polar functional groups. Its molecular structure suggests potential applications in pharmaceuticals or as an intermediate in organic synthesis, particularly in the development of biologically active compounds. Additionally, the presence of both a ketone and nitro group may impart unique chemical properties, such as increased acidity or reactivity under certain conditions. Safety and handling precautions should be observed, as with many halogenated and nitro compounds, due to potential toxicity and environmental concerns.

CAS 487058-74-2

5-chloro-1-(3-nitrophenyl)pentan-1-one

5-Chloro-1-(3-nitrophenyl)-1-oxopentane

Ref: 10-F203712