5-Chloro-1-(3,4-dimethoxyphenyl)pentan-1-one is an organic compound characterized by its structural features, which include a pentanone backbone with a chloro substituent and a 3,4-dimethoxyphenyl group. This compound typically exhibits a moderate molecular weight and is likely to be a solid or liquid at room temperature, depending on its specific physical properties. The presence of the chloro group introduces unique reactivity, potentially allowing for nucleophilic substitution reactions. The methoxy groups on the phenyl ring enhance the compound's electron-donating characteristics, which can influence its reactivity and solubility in various solvents. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry and pharmacology. Its synthesis may involve standard organic reactions such as Friedel-Crafts acylation or nucleophilic substitution. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks or environmental hazards. Proper characterization techniques, such as NMR and mass spectrometry, are essential for confirming its structure and purity.

5-chloro-1-(3,4-dimethoxyphenyl)pentan-1-one

33245-77-1: 5-Chloro-1-(3,4-dimethoxyphenyl)pentan-1-one is an organic compound characterized by its structural features, which include a pentanone backbone with a chloro substituent and a 3,4-dimethoxyphenyl group. This compound typically exhibits a moderate molecular weight and is likely to be a solid or liquid at room temperature, depending on its specific physical properties. The presence of the chloro group introduces unique reactivity, potentially allowing for nucleophilic substitution reactions. The methoxy groups on the phenyl ring enhance the compound's electron-donating characteristics, which can influence its reactivity and solubility in various solvents. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry and pharmacology. Its synthesis may involve standard organic reactions such as Friedel-Crafts acylation or nucleophilic substitution. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks or environmental hazards. Proper characterization techniques, such as NMR and mass spectrometry, are essential for confirming its structure and purity.

CAS 33245-77-1

5-chloro-1-(3,4-dimethoxyphenyl)pentan-1-one

1-Chloro-5-(3,4-dimethoxyphenyl)-5-oxopentane

Ref: 10-F206967