Ethyl 6-hydroxy-5-nitro-4-oxo-1,4-dihydropyridine-3-carboxylate, with the CAS number 6317-97-1, is a chemical compound that belongs to the class of dihydropyridine derivatives. This compound features a pyridine ring with various functional groups, including a hydroxyl group, a nitro group, and a carboxylate ester, which contribute to its chemical reactivity and potential biological activity. The presence of the nitro group suggests that it may exhibit unique electronic properties, while the carboxylate moiety can participate in various chemical reactions, including esterification and acid-base reactions. The compound is typically characterized by its solid state at room temperature and may exhibit solubility in polar organic solvents. Its structural features indicate potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activities often associated with dihydropyridine derivatives, such as calcium channel modulation. However, specific properties such as melting point, boiling point, and spectral data would require empirical measurement or literature reference for precise characterization.

ethyl 6-hydroxy-5-nitro-4-oxo-1,4-dihydropyridine-3-carboxylate

6317-97-1: Ethyl 6-hydroxy-5-nitro-4-oxo-1,4-dihydropyridine-3-carboxylate, with the CAS number 6317-97-1, is a chemical compound that belongs to the class of dihydropyridine derivatives. This compound features a pyridine ring with various functional groups, including a hydroxyl group, a nitro group, and a carboxylate ester, which contribute to its chemical reactivity and potential biological activity. The presence of the nitro group suggests that it may exhibit unique electronic properties, while the carboxylate moiety can participate in various chemical reactions, including esterification and acid-base reactions. The compound is typically characterized by its solid state at room temperature and may exhibit solubility in polar organic solvents. Its structural features indicate potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activities often associated with dihydropyridine derivatives, such as calcium channel modulation. However, specific properties such as melting point, boiling point, and spectral data would require empirical measurement or literature reference for precise characterization.

CAS 6317-97-1

ethyl 6-hydroxy-5-nitro-4-oxo-1,4-dihydropyridine-3-carboxylate

4,6-Dihydroxy-5-nitropyridine-3-carboxylic acid ethyl ester

Ref: IN-DA00EG4R

Ethyl 4,6-dihydroxy-5-nitronicotinate

Ref: 54-OR01968

Ethyl 4,6-Dihydroxy-5-nitronicotinate

Ref: 10-F066894