4(1H)-Quinolinone, 6-bromo-2,3-dihydro- is a chemical compound characterized by its quinolinone structure, which features a fused bicyclic system containing a nitrogen atom. This compound is notable for the presence of a bromine atom at the 6-position of the quinolinone ring, which can influence its reactivity and biological activity. The dihydro form indicates that the compound has two hydrogen atoms added to the ring, typically resulting in a saturated structure that can affect its physical properties, such as solubility and melting point. This compound may exhibit various pharmacological activities, making it of interest in medicinal chemistry. Its molecular formula and structure suggest potential applications in drug development, particularly in the synthesis of novel therapeutic agents. Additionally, the presence of the bromine substituent can enhance the compound's lipophilicity, potentially improving its bioavailability. As with many heterocyclic compounds, the specific interactions and reactivity of 4(1H)-Quinolinone, 6-bromo-2,3-dihydro- can be explored further in the context of organic synthesis and medicinal applications.

4(1H)-Quinolinone,6-bromo-2,3-dihydro-

76228-06-3: 4(1H)-Quinolone,6-bromo-2,3-dihydro- (7CI), 6-Bromo-2,3-dihydroquinolin-4(1H)-one, 6-Bromo-2,3-dihydro-1H-quinolin-4-one

6-Bromo-2,3-dihydroquinolin-4(1H)-one

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CAS 76228-06-3: 4(1H)-Quinolinone,6-bromo-2,3-dihydro-

6-Bromo-2,3-dihydroquinolin-4(1H)-one

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6-Bromo-2,3-dihydroquinolin-4(1H)-one

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6-Bromo-2,3-dihydroquinolin-4(1H)-one

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6-Bromo-2,3-Dihydroquinolin-4(1H)-One

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