8-Fluoroquinoline-2-carbaldehyde is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a fluorine atom at the 8-position of the quinoline ring imparts unique electronic and steric properties, influencing its reactivity and potential applications. The aldehyde functional group (-CHO) at the 2-position contributes to its reactivity, making it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. This compound is typically a yellow to brown solid and is soluble in organic solvents. Its chemical behavior can be attributed to the electron-withdrawing nature of the fluorine atom, which can enhance electrophilic reactivity. Additionally, 8-fluoroquinoline-2-carbaldehyde may exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling, as with many organic compounds, it may pose health risks if not managed properly. Overall, its unique structure and functional groups make it a compound of interest in various chemical research fields.

8-fluoroquinoline-2-carbaldehyde

904369-10-4: 8-Fluoroquinoline-2-carbaldehyde is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a fluorine atom at the 8-position of the quinoline ring imparts unique electronic and steric properties, influencing its reactivity and potential applications. The aldehyde functional group (-CHO) at the 2-position contributes to its reactivity, making it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. This compound is typically a yellow to brown solid and is soluble in organic solvents. Its chemical behavior can be attributed to the electron-withdrawing nature of the fluorine atom, which can enhance electrophilic reactivity. Additionally, 8-fluoroquinoline-2-carbaldehyde may exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling, as with many organic compounds, it may pose health risks if not managed properly. Overall, its unique structure and functional groups make it a compound of interest in various chemical research fields.

CAS 904369-10-4

8-fluoroquinoline-2-carbaldehyde

8-Fluoroquinoline-2-carbaldehyde

Ref: IN-DA00GVNT

8-Fluoroquinoline-2-carbaldehyde

Ref: 54-PC905560

8-Fluoroquinoline-2-carbaldehyde

Ref: 10-F228357