3,5-Diiodo-4-hydroxyacetophenone
- Molecular formula
- C8H6I2O2
- CAS Number
- 13329-34-5
- IUPAC Name
- 1-(4-hydroxy-3,5-diiodo-phenyl)ethanone
- Molecular Weight
- 388.94g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 3.0700g/cm3
- Synonyms
- 1-(4-hydroxy-3, 5-diiodophenyl)ethanone
Identification
Interesting Facts about 1-(4-hydroxy-3,5-diiodo-phenyl)ethanone
This compound belongs to the family of halogenated phenols, which are known for their diverse applications in various fields such as pharmaceuticals, agrochemicals, and materials science. The intriguing aspect of 1-(4-hydroxy-3,5-diiodo-phenyl)ethanone lies in its unique chemical structure and the influence of its halogen atoms:
- Halogen Influence: The presence of iodine atoms in the molecular structure significantly increases the compound's reactivity and molecular stability. This can lead to various interesting chemical behaviors, especially in reactions involving electrophiles.
- Biological Activity: Compounds with hydroxyl and halogen substituents often exhibit considerable biological activity. This particular compound has potential as a candidate for research in medicinal chemistry, where it may demonstrate antibacterial or anticancer properties.
- Synthesis Interest: The synthesis of halogenated intermediates can be a challenge, making this compound a valuable target for organic synthesis methodologies, such as electrophilic aromatic substitution.
- Environmental Considerations: Like many halogenated compounds, 1-(4-hydroxy-3,5-diiodo-phenyl)ethanone can be subject to environmental scrutiny due to the persistence and potential toxicity of its halogenated derivatives.
In a world increasingly focused on sustainable chemistry, the study of such halogenated compounds is crucial. As noted by researchers, “Understanding the properties and potential applications of halogenated compounds opens the door to innovations in materials and pharmaceuticals.” This compound exemplifies a broader category of biologically and chemically important molecules that continue to inspire scientific inquiry.
Ultimately, 1-(4-hydroxy-3,5-diiodo-phenyl)ethanone serves as both a fascinating subject of study and a reminder of the importance of responsible chemical research.