2-Bromo-3-fluoro-6-methoxybenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. The presence of bromine and fluorine substituents on the benzene ring, along with a methoxy group, contributes to its unique chemical properties. This compound typically exhibits moderate polarity due to the electronegative halogen atoms and the methoxy group, which can influence its solubility in various solvents. The bromine and fluorine atoms can also affect the compound's reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, the methoxy group can serve as an electron-donating group, enhancing the reactivity of the aromatic ring. 2-Bromo-3-fluoro-6-methoxybenzaldehyde may be utilized in synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals, due to its functional groups that allow for further derivatization. Its specific properties, such as melting point, boiling point, and spectral characteristics, would need to be referenced from experimental data for precise applications.

2-bromo-3-fluoro-6-methoxybenzaldehyde

1780200-30-7: 2-Bromo-3-fluoro-6-methoxybenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. The presence of bromine and fluorine substituents on the benzene ring, along with a methoxy group, contributes to its unique chemical properties. This compound typically exhibits moderate polarity due to the electronegative halogen atoms and the methoxy group, which can influence its solubility in various solvents. The bromine and fluorine atoms can also affect the compound's reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, the methoxy group can serve as an electron-donating group, enhancing the reactivity of the aromatic ring. 2-Bromo-3-fluoro-6-methoxybenzaldehyde may be utilized in synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals, due to its functional groups that allow for further derivatization. Its specific properties, such as melting point, boiling point, and spectral characteristics, would need to be referenced from experimental data for precise applications.

CAS 1780200-30-7

2-bromo-3-fluoro-6-methoxybenzaldehyde

2-Bromo-3-fluoro-6-methoxybenzaldehyde

Ref: IN-DA01DFBU

2-Bromo-3-fluoro-6-methoxybenzaldehyde

Ref: 54-PC110315

2-BROMO-3-FLUORO-6-METHOXYBENZALDEHYDE

Ref: 10-F822530

2-Bromo-3-fluoro-6-methoxybenzaldehyde

Ref: 3D-FWC20030