4,4′-Difluorodiphenylmethanone CAS:345-92-6
Catalog Number | XD94847 |
Product Name | 4,4′-Difluorodiphenylmethanone |
CAS | 345-92-6 |
Molecular Formula | C13H8F2O |
Molecular Weight | 218.2 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
4,4'-Difluorodiphenylmethanone is an organic compound with a wide range of effects and applications in various fields. This compound is part of the ketone family, characterized by its carbonyl group (C=O) attached to two aromatic rings.One of the notable effects of 4,4'-Difluorodiphenylmethanone is its electron-withdrawing property due to the presence of the carbonyl group. This electron deficiency makes the compound a strong electrophile, enabling it to participate in various reactions. For instance, it can undergo nucleophilic addition reactions with nucleophiles such as amines or organometallic compounds. This allows for the synthesis of a range of organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals.Moreover, the fluorine atoms attached to the aromatic rings in 4,4'-Difluorodiphenylmethanone contribute to its unique properties and effects. Fluorine is known for its high electronegativity, which can enhance chemical stability and alter the reactivity of molecules. In the case of 4,4'-Difluorodiphenylmethanone, the presence of fluorine atoms can increase chemical resistance, improve thermal stability, and modify the electronic properties of the compound, making it useful in various applications.Additionally, 4,4'-Difluorodiphenylmethanone can act as a building block in organic synthesis. Its two aromatic rings provide opportunities for further functionalization through various reactions, such as substitution or addition reactions, allowing for the introduction of different functional groups. This versatility makes it a valuable precursor in the synthesis of complex organic compounds with desired properties.Furthermore, 4,4'-Difluorodiphenylmethanone has been found to exhibit antimicrobial and anticancer activity. Studies have shown that this compound possesses inhibitory effects against certain bacterial and fungal strains, making it a potential candidate for the development of antimicrobial agents. Additionally, due to the involvement of ketones in various biological processes, 4,4'-Difluorodiphenylmethanone and its derivatives have shown promise in cancer research, potentially serving as lead compounds for drug development.It is important to note that while 4,4'-Difluorodiphenylmethanone has displayed beneficial effects in various applications, proper handling and safety precautions are crucial. As with any compound, it is necessary to follow appropriate protocols to minimize health risks and ensure safe utilization.In conclusion, 4,4'-Difluorodiphenylmethanone is a versatile organic compound with notable effects and applications. Its electron-withdrawing property, combined with the presence of fluorine atoms, contributes to its reactivity and unique properties. The compound can be used as a building block in synthesis, exhibits antimicrobial and anticancer activity, and holds potential for further exploration in pharmaceutical and agricultural research.