6-Chloro-N-(3-chlorophenyl)pyridine-3-carboxamide, with the CAS number 877836-74-3, is a chemical compound characterized by its pyridine ring structure, which is substituted at the 6-position with a chlorine atom and at the 3-position with a carboxamide group. The presence of a 3-chlorophenyl group attached to the nitrogen of the carboxamide enhances its potential for biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. Its molecular structure suggests potential interactions with biological targets, making it of interest in medicinal chemistry and drug development. The chlorine substituents may influence its electronic properties and reactivity, potentially affecting its pharmacokinetics and pharmacodynamics. As with many compounds containing halogens and heterocycles, it may also exhibit specific characteristics such as lipophilicity and the ability to form hydrogen bonds, which are crucial for its biological activity and interactions.

6-chloro-N-(3-chlorophenyl)pyridine-3-carboxamide

877836-74-3: 6-Chloro-N-(3-chlorophenyl)pyridine-3-carboxamide, with the CAS number 877836-74-3, is a chemical compound characterized by its pyridine ring structure, which is substituted at the 6-position with a chlorine atom and at the 3-position with a carboxamide group. The presence of a 3-chlorophenyl group attached to the nitrogen of the carboxamide enhances its potential for biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. Its molecular structure suggests potential interactions with biological targets, making it of interest in medicinal chemistry and drug development. The chlorine substituents may influence its electronic properties and reactivity, potentially affecting its pharmacokinetics and pharmacodynamics. As with many compounds containing halogens and heterocycles, it may also exhibit specific characteristics such as lipophilicity and the ability to form hydrogen bonds, which are crucial for its biological activity and interactions.

CAS 877836-74-3

6-chloro-N-(3-chlorophenyl)pyridine-3-carboxamide

6-Chloro-N-(3-chlorophenyl)pyridine-3-carboxamide

Ref: 3D-CKB83674