4(1H)-Pyridinone, 3-iodo- is a heterocyclic organic compound characterized by a pyridinone structure, which includes a pyridine ring fused with a carbonyl group. The presence of an iodine atom at the 3-position of the pyridinone ring significantly influences its chemical reactivity and properties. This compound typically exhibits a pale yellow to brownish appearance and is soluble in polar organic solvents. It may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the electron-withdrawing nature of the iodine substituent. The compound is of interest in medicinal chemistry and material science, as derivatives of pyridinones often exhibit biological activity and can serve as precursors for the synthesis of more complex molecules. Additionally, its iodine content may impart unique properties, such as enhanced X-ray contrast or specific interactions in biological systems. Safety data should be consulted, as halogenated compounds can pose health risks and environmental concerns.

4(1H)-Pyridinone, 3-iodo-

98136-83-5: 4(1H)-Pyridinone, 3-iodo- is a heterocyclic organic compound characterized by a pyridinone structure, which includes a pyridine ring fused with a carbonyl group. The presence of an iodine atom at the 3-position of the pyridinone ring significantly influences its chemical reactivity and properties. This compound typically exhibits a pale yellow to brownish appearance and is soluble in polar organic solvents. It may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the electron-withdrawing nature of the iodine substituent. The compound is of interest in medicinal chemistry and material science, as derivatives of pyridinones often exhibit biological activity and can serve as precursors for the synthesis of more complex molecules. Additionally, its iodine content may impart unique properties, such as enhanced X-ray contrast or specific interactions in biological systems. Safety data should be consulted, as halogenated compounds can pose health risks and environmental concerns.

CAS 98136-83-5

4(1H)-Pyridinone, 3-iodo-