2-(4-Chlorophenyl)quinoline-4-carbohydrazide is an organic compound characterized by its unique structure, which includes a quinoline moiety and a hydrazide functional group. This compound typically exhibits a solid state at room temperature and is often used in various chemical and biological applications, including medicinal chemistry and as a potential pharmacological agent. The presence of the 4-chlorophenyl group may impart specific electronic and steric properties, influencing its reactivity and interaction with biological targets. The hydrazide functionality can participate in various chemical reactions, such as hydrazone formation and condensation reactions, making it versatile in synthetic chemistry. Additionally, compounds of this nature may exhibit biological activities, including antimicrobial or anticancer properties, although specific biological data would depend on empirical studies. Safety and handling precautions should be observed due to the potential toxicity associated with halogenated compounds. Overall, 2-(4-chlorophenyl)quinoline-4-carbohydrazide represents a significant compound for research and development in the field of organic and medicinal chemistry.

2-(4-CHLOROPHENYL)QUINOLINE-4-CARBOHYDRAZIDE

884837-13-2: 2-(4-Chlorophenyl)quinoline-4-carbohydrazide is an organic compound characterized by its unique structure, which includes a quinoline moiety and a hydrazide functional group. This compound typically exhibits a solid state at room temperature and is often used in various chemical and biological applications, including medicinal chemistry and as a potential pharmacological agent. The presence of the 4-chlorophenyl group may impart specific electronic and steric properties, influencing its reactivity and interaction with biological targets. The hydrazide functionality can participate in various chemical reactions, such as hydrazone formation and condensation reactions, making it versatile in synthetic chemistry. Additionally, compounds of this nature may exhibit biological activities, including antimicrobial or anticancer properties, although specific biological data would depend on empirical studies. Safety and handling precautions should be observed due to the potential toxicity associated with halogenated compounds. Overall, 2-(4-chlorophenyl)quinoline-4-carbohydrazide represents a significant compound for research and development in the field of organic and medicinal chemistry.

CAS 884837-13-2

2-(4-CHLOROPHENYL)QUINOLINE-4-CARBOHYDRAZIDE

2-(4-Chlorophenyl)-quinoline-4-carboxylic acidhydrazide

Ref: 10-F014615