2-(3-Chlorophenyl)ethanethioamide is an organic compound characterized by its thioamide functional group, which features a sulfur atom bonded to a carbonyl carbon. This compound contains a 3-chlorophenyl group, indicating the presence of a chlorine atom on the aromatic ring, which can influence its reactivity and biological activity. The thioamide group typically exhibits properties similar to amides but with distinct characteristics due to the presence of sulfur, such as altered hydrogen bonding capabilities and potential for different reactivity patterns. The compound may exhibit moderate solubility in organic solvents and limited solubility in water, typical of many thioamides. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as thioamides can serve as precursors or intermediates in the synthesis of biologically active molecules. Additionally, the presence of the chlorophenyl moiety may enhance its lipophilicity, influencing its pharmacokinetic properties. Overall, 2-(3-chlorophenyl)ethanethioamide is a compound of interest for further study in various chemical and biological contexts.

2-(3-chlorophenyl)ethanethioamide

834861-72-2: 2-(3-Chlorophenyl)ethanethioamide is an organic compound characterized by its thioamide functional group, which features a sulfur atom bonded to a carbonyl carbon. This compound contains a 3-chlorophenyl group, indicating the presence of a chlorine atom on the aromatic ring, which can influence its reactivity and biological activity. The thioamide group typically exhibits properties similar to amides but with distinct characteristics due to the presence of sulfur, such as altered hydrogen bonding capabilities and potential for different reactivity patterns. The compound may exhibit moderate solubility in organic solvents and limited solubility in water, typical of many thioamides. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as thioamides can serve as precursors or intermediates in the synthesis of biologically active molecules. Additionally, the presence of the chlorophenyl moiety may enhance its lipophilicity, influencing its pharmacokinetic properties. Overall, 2-(3-chlorophenyl)ethanethioamide is a compound of interest for further study in various chemical and biological contexts.

CAS 834861-72-2

2-(3-chlorophenyl)ethanethioamide

2-(3-Chlorophenyl)ethanethioamide

Ref: IN-DA004V9J

2-(3-Chlorophenyl)ethanethioamide

Ref: 54-OR954557