2-Difluoromethoxy-6-fluorobenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group and two fluorine atoms attached to the benzene ring. The presence of the methoxy group (–OCH3) and the difluoromethyl group (–CF2) contributes to its unique chemical properties, influencing its reactivity and polarity. This compound is typically a colorless to pale yellow liquid or solid, depending on its state at room temperature. It is likely to exhibit moderate solubility in organic solvents due to the presence of both polar and nonpolar functional groups. The fluorine substituents can enhance the compound's stability and lipophilicity, making it of interest in various applications, including pharmaceuticals and agrochemicals. Additionally, the compound may participate in electrophilic aromatic substitution reactions due to the electron-withdrawing nature of the fluorine atoms, which can affect the reactivity of the aromatic ring. Safety data should be consulted for handling and storage, as fluorinated compounds can pose specific health and environmental risks.

2-difluoroMethoxy-6-fluorobenzaldehyde

1214333-68-2: 2-Difluoromethoxy-6-fluorobenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group and two fluorine atoms attached to the benzene ring. The presence of the methoxy group (–OCH3) and the difluoromethyl group (–CF2) contributes to its unique chemical properties, influencing its reactivity and polarity. This compound is typically a colorless to pale yellow liquid or solid, depending on its state at room temperature. It is likely to exhibit moderate solubility in organic solvents due to the presence of both polar and nonpolar functional groups. The fluorine substituents can enhance the compound's stability and lipophilicity, making it of interest in various applications, including pharmaceuticals and agrochemicals. Additionally, the compound may participate in electrophilic aromatic substitution reactions due to the electron-withdrawing nature of the fluorine atoms, which can affect the reactivity of the aromatic ring. Safety data should be consulted for handling and storage, as fluorinated compounds can pose specific health and environmental risks.

Benzaldehyde, 2-(difluoromethoxy)-6-fluoro-

<p>2-(Difluoromethoxy)-6-fluorobenzaldehyde</p>

CAS 1214333-68-2

2-difluoroMethoxy-6-fluorobenzaldehyde

Benzaldehyde, 2-(difluoromethoxy)-6-fluoro-

Ref: IN-DA0014T0

2-(Difluoromethoxy)-6-fluorobenzaldehyde

Ref: 54-PC502196

2-(Difluoromethoxy)-6-fluorobenzaldehyde

Ref: 10-F216787