2(1H)-Quinolinone, 3-fluoro- is a chemical compound characterized by its quinolinone structure, which features a fused bicyclic system comprising a benzene ring and a pyridine ring. The presence of a fluorine atom at the 3-position of the quinolinone moiety introduces unique electronic and steric properties, potentially influencing its reactivity and interactions with biological targets. This compound is typically a pale yellow to off-white solid and is soluble in organic solvents. It may exhibit various biological activities, making it of interest in medicinal chemistry and drug development. The fluorine substitution can enhance lipophilicity and metabolic stability, which are desirable traits in pharmaceutical applications. Additionally, the compound's properties can be further explored through techniques such as NMR spectroscopy and mass spectrometry for structural elucidation and purity assessment. As with many quinolinone derivatives, it may also serve as a scaffold for the synthesis of more complex molecules in research settings. Safety and handling precautions should be observed, as with all chemical substances.

2(1H)-Quinolinone, 3-fluoro-

124467-22-7: 2(1H)-Quinolinone, 3-fluoro- is a chemical compound characterized by its quinolinone structure, which features a fused bicyclic system comprising a benzene ring and a pyridine ring. The presence of a fluorine atom at the 3-position of the quinolinone moiety introduces unique electronic and steric properties, potentially influencing its reactivity and interactions with biological targets. This compound is typically a pale yellow to off-white solid and is soluble in organic solvents. It may exhibit various biological activities, making it of interest in medicinal chemistry and drug development. The fluorine substitution can enhance lipophilicity and metabolic stability, which are desirable traits in pharmaceutical applications. Additionally, the compound's properties can be further explored through techniques such as NMR spectroscopy and mass spectrometry for structural elucidation and purity assessment. As with many quinolinone derivatives, it may also serve as a scaffold for the synthesis of more complex molecules in research settings. Safety and handling precautions should be observed, as with all chemical substances.

CAS 124467-22-7

2(1H)-Quinolinone, 3-fluoro-

3-Fluoroquinolin-2(1H)-one

Ref: IN-DA000M2D

3-Fluoro-1,2-dihydroquinolin-2-one

Ref: 3D-ZEA46722