3-Chloro-5-fluoro-4-methoxybenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. The presence of chlorine and fluorine substituents on the benzene ring contributes to its unique reactivity and physical properties. The methoxy group (-OCH3) enhances its solubility in organic solvents and can influence its electronic properties, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. This compound is typically used in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to serve as an intermediate in the synthesis of more complex molecules. Its specific reactivity can be attributed to the electron-withdrawing effects of the halogen substituents, which can stabilize certain reaction intermediates. Additionally, the compound's physical properties, such as melting point and boiling point, are influenced by its molecular structure and the presence of functional groups. Safety data should be consulted for handling and storage, as with all chemical substances.

3-CHLORO-5-FLUORO-4-METHOXYBENZALDEHYDE

177994-49-9: 3-Chloro-5-fluoro-4-methoxybenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. The presence of chlorine and fluorine substituents on the benzene ring contributes to its unique reactivity and physical properties. The methoxy group (-OCH3) enhances its solubility in organic solvents and can influence its electronic properties, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. This compound is typically used in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to serve as an intermediate in the synthesis of more complex molecules. Its specific reactivity can be attributed to the electron-withdrawing effects of the halogen substituents, which can stabilize certain reaction intermediates. Additionally, the compound's physical properties, such as melting point and boiling point, are influenced by its molecular structure and the presence of functional groups. Safety data should be consulted for handling and storage, as with all chemical substances.

CAS 177994-49-9

3-CHLORO-5-FLUORO-4-METHOXYBENZALDEHYDE

Benzaldehyde, 3-chloro-5-fluoro-4-methoxy-

Ref: IN-DA0025OX

3-Chloro-5-fluoro-4-methoxybenzaldehyde

Ref: 54-PC302536

3-Chloro-5-fluoro-4-methoxybenzaldehyde

Ref: 10-F342339