3-Fluoro-5-methoxypyridine-4-carbaldehyde is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a fluorine atom at the 3-position and a methoxy group at the 5-position contributes to its unique chemical properties, influencing its reactivity and polarity. The aldehyde functional group at the 4-position is notable for its reactivity, particularly in condensation reactions and as a precursor for various synthetic pathways. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in organic solvents, which makes it useful in various chemical reactions and applications, including medicinal chemistry and the synthesis of more complex organic molecules. The presence of both electron-withdrawing (fluorine) and electron-donating (methoxy) groups can significantly affect the compound's electronic properties, making it a valuable intermediate in the development of pharmaceuticals and agrochemicals. Safety and handling precautions should be observed due to potential toxicity and reactivity associated with aldehyde compounds.

3-Fluoro-5-Methoxypyridine-4-carbaldehyde

1256792-34-3: 3-Fluoro-5-methoxypyridine-4-carbaldehyde is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a fluorine atom at the 3-position and a methoxy group at the 5-position contributes to its unique chemical properties, influencing its reactivity and polarity. The aldehyde functional group at the 4-position is notable for its reactivity, particularly in condensation reactions and as a precursor for various synthetic pathways. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in organic solvents, which makes it useful in various chemical reactions and applications, including medicinal chemistry and the synthesis of more complex organic molecules. The presence of both electron-withdrawing (fluorine) and electron-donating (methoxy) groups can significantly affect the compound's electronic properties, making it a valuable intermediate in the development of pharmaceuticals and agrochemicals. Safety and handling precautions should be observed due to potential toxicity and reactivity associated with aldehyde compounds.

CAS 1256792-34-3

3-Fluoro-5-Methoxypyridine-4-carbaldehyde

3-Fluoro-5-methoxyisonicotinaldehyde

Ref: IN-DA000OD8

3-Fluoro-5-methoxyisonicotinaldehyde

Ref: 54-PC907544

3-Fluoro-5-methoxyisonicotinaldehyde

Ref: 10-F461981