3-(Difluoromethoxy)-4-fluorobenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group and two fluorine atoms attached to the aromatic ring. The presence of the difluoromethoxy group introduces unique electronic and steric properties, influencing its reactivity and interactions with other molecules. This compound is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is soluble in organic solvents, reflecting its non-polar characteristics, while its reactivity can be attributed to the aldehyde functional group, which is prone to nucleophilic attack. The fluorine substituents enhance the compound's lipophilicity and may affect its biological activity, making it of interest in medicinal chemistry and material science. Safety data should be consulted for handling, as fluorinated compounds can exhibit toxicity and environmental persistence. Overall, 3-(difluoromethoxy)-4-fluorobenzaldehyde is a valuable compound in synthetic organic chemistry and research applications.

3-(difluoromethoxy)-4-fluorobenzaldehyde

1214367-20-0: 3-(Difluoromethoxy)-4-fluorobenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group and two fluorine atoms attached to the aromatic ring. The presence of the difluoromethoxy group introduces unique electronic and steric properties, influencing its reactivity and interactions with other molecules. This compound is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is soluble in organic solvents, reflecting its non-polar characteristics, while its reactivity can be attributed to the aldehyde functional group, which is prone to nucleophilic attack. The fluorine substituents enhance the compound's lipophilicity and may affect its biological activity, making it of interest in medicinal chemistry and material science. Safety data should be consulted for handling, as fluorinated compounds can exhibit toxicity and environmental persistence. Overall, 3-(difluoromethoxy)-4-fluorobenzaldehyde is a valuable compound in synthetic organic chemistry and research applications.

Benzaldehyde, 3-(difluoromethoxy)-4-fluoro-

<p>3-(Difluoromethoxy)-4-fluorobenzaldehyde</p>

CAS 1214367-20-0

3-(difluoromethoxy)-4-fluorobenzaldehyde

Benzaldehyde, 3-(difluoromethoxy)-4-fluoro-

Ref: IN-DA0014WE

3-(Difluoromethoxy)-4-fluorobenzaldehyde

Ref: 54-PC508024

3-(Difluoromethoxy)-4-fluorobenzaldehyde

Ref: 10-F544681