4-Fluoro-3-iodobenzaldehyde is an organic compound characterized by the presence of both a fluorine and an iodine atom on a benzaldehyde ring. Its molecular structure features a benzene ring substituted with a formyl group (-CHO), a fluorine atom at the para position (4-position), and an iodine atom at the meta position (3-position). This compound is typically a pale yellow to brown solid and is known for its reactivity due to the presence of the aldehyde functional group, which can participate in various chemical reactions such as nucleophilic addition and condensation. The presence of halogens (fluorine and iodine) can influence the compound's electronic properties, making it useful in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals. Additionally, 4-Fluoro-3-iodobenzaldehyde may exhibit unique physical properties, such as solubility in organic solvents, and its reactivity can be leveraged in cross-coupling reactions or as a building block for more complex molecules. Safety precautions should be taken when handling this compound due to its potential toxicity and reactivity.

4-Fluoro-3-iodobenzaldehyde

227609-88-3: 4-Fluoro-3-iodobenzaldehyde is an organic compound characterized by the presence of both a fluorine and an iodine atom on a benzaldehyde ring. Its molecular structure features a benzene ring substituted with a formyl group (-CHO), a fluorine atom at the para position (4-position), and an iodine atom at the meta position (3-position). This compound is typically a pale yellow to brown solid and is known for its reactivity due to the presence of the aldehyde functional group, which can participate in various chemical reactions such as nucleophilic addition and condensation. The presence of halogens (fluorine and iodine) can influence the compound's electronic properties, making it useful in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals. Additionally, 4-Fluoro-3-iodobenzaldehyde may exhibit unique physical properties, such as solubility in organic solvents, and its reactivity can be leveraged in cross-coupling reactions or as a building block for more complex molecules. Safety precautions should be taken when handling this compound due to its potential toxicity and reactivity.

CAS 227609-88-3

4-Fluoro-3-iodobenzaldehyde

4-FLUORO-3-IODOBENZALDEHYDE

Ref: IN-DA00BEOM

4-Fluoro-3-iodobenzaldehyde

Ref: 54-PC9099

4-Fluoro-3-iodobenzaldehyde

Ref: 10-F050132