2-(3-Chlorophenyl)-1-hydrazinecarbothioamide, with the CAS number 828-11-5, is an organic compound characterized by the presence of a hydrazine functional group and a thioamide moiety. This compound features a chlorophenyl group, which contributes to its potential biological activity and chemical reactivity. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the hydrazine group suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to form various derivatives. Additionally, the thioamide functional group can participate in diverse chemical reactions, including nucleophilic substitutions and coordination with metal ions. The chlorophenyl substituent may influence the compound's electronic properties and steric effects, impacting its reactivity and interactions with biological targets. Safety data should be consulted, as compounds containing hydrazine derivatives can be hazardous and may require careful handling. Overall, this compound's unique structure positions it as a subject of interest in both synthetic and applied chemistry.

2-(3-CHLOROPHENYL)-1-HYDRAZINECARBOTHIOAMIDE

828-11-5: 2-(3-Chlorophenyl)-1-hydrazinecarbothioamide, with the CAS number 828-11-5, is an organic compound characterized by the presence of a hydrazine functional group and a thioamide moiety. This compound features a chlorophenyl group, which contributes to its potential biological activity and chemical reactivity. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the hydrazine group suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to form various derivatives. Additionally, the thioamide functional group can participate in diverse chemical reactions, including nucleophilic substitutions and coordination with metal ions. The chlorophenyl substituent may influence the compound's electronic properties and steric effects, impacting its reactivity and interactions with biological targets. Safety data should be consulted, as compounds containing hydrazine derivatives can be hazardous and may require careful handling. Overall, this compound's unique structure positions it as a subject of interest in both synthetic and applied chemistry.

CAS 828-11-5

2-(3-CHLOROPHENYL)-1-HYDRAZINECARBOTHIOAMIDE