CAS 207976-92-9

2(1H)-Pyridinone, 3-chloro-5,6-dihydro-

Description:

2(1H)-Pyridinone, 3-chloro-5,6-dihydro- is a chemical compound characterized by its pyridinone structure, which features a pyridine ring with a ketone functional group. The presence of a chlorine atom at the 3-position and the saturation of the 5 and 6 positions contribute to its unique reactivity and properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the polar carbonyl group. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as derivatives of pyridinones are often explored for their biological activity. The compound may also participate in various chemical reactions, including nucleophilic substitutions and cyclization processes, making it of interest in synthetic organic chemistry. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 2(1H)-Pyridinone, 3-chloro-5,6-dihydro- represents a versatile scaffold in chemical research.

Formula: C₅H₆ClNO

3-Chloro-5,6-dihydropyridin-2(1H)-one

CAS: 207976-92-9

Formula: C₅H₆ClNO

Molecular weight: 131.5602

Ref: IN-DA002JE9

3-chloro-1,2,5,6-tetrahydropyridin-2-one

CAS: 207976-92-9

3-chloro-1,2,5,6-tetrahydropyridin-2-one

Formula: C₅H₆ClNO

Purity: ≥95%

Color and Shape: light brown crystalline powder

Molecular weight: 131.56g/mol

Ref: 54-OR97143

3-CHLORO-5,6-DIHYDROPYRIDIN-2(1H)-ONE

CAS: 207976-92-9

Formula: C₅H₆ClNO

Purity: 95.0%

Molecular weight: 131.56

Ref: 10-F473261

3-Chloro-5,6-dihydropyridin-2(1H)-one

CAS: 207976-92-9

3-Chloro-5,6-dihydropyridin-2(1H)-one is a chemical compound that has been shown to have antiparasitic properties against Leishmania. The molecule is able to inhibit the growth of promastigotes and surface-exposed amastigotes of Leishmania infantum by inhibiting the synthesis of fatty acids. 3-Chloro-5,6-dihydropyridin-2(1H)-one also blocks the synthesis of glutathione, a major antioxidant in cells that protects against oxidative damage. This compound has been shown to be efficacious in vitro against cancer cells, including A549 cells.

Formula: C₅H₆NOCl

Purity: Min. 95%

Molecular weight: 131.56 g/mol

Ref: 3D-HIA97692