4-Chloropyridine-3-carboxamide, with the CAS number 7418-70-4, is an organic compound characterized by its pyridine ring structure substituted with a chlorine atom and a carboxamide functional group. This compound typically appears as a solid at room temperature and is soluble in polar solvents, reflecting its ability to engage in hydrogen bonding due to the presence of the carboxamide group. The chlorine substituent can influence the compound's reactivity and polarity, making it useful in various chemical syntheses and applications. It is often employed in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. The presence of both the chloropyridine and carboxamide functionalities allows for diverse chemical transformations, including nucleophilic substitutions and coupling reactions. Safety data sheets should be consulted for handling and storage guidelines, as with many chemical substances, to ensure safe laboratory practices. Overall, 4-chloropyridine-3-carboxamide is a valuable compound in organic chemistry and medicinal chemistry contexts.

4-chloropyridine-3-carboxamide

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4-Chloronicotinamide is a noncatalytic, dinucleotide, pyridine ring that is used in the treatment of cancer. It is synthesized from 2-chloronicotinic acid and amide by nucleophilic substitution. 4-Chloronicotinamide has low activity against oxazoles and pyridine but high activity against nucleophiles such as DNA, RNA, and proteins. This compound was labeled with 14C to study its biosynthesis in bacteria.

CAS 7418-70-4: 4-chloropyridine-3-carboxamide

4-Chloronicotinamide

Ref: 3D-FC142704

4-Chloronicotinamide

Ref: IN-DA005DE7

4-Chloronicotinamide

Ref: 10-F068383

4-Chloropyridine-3-carboxamide

Ref: 54-OR951010