Trifluoromethoxybenzene CAS:456-55-3
Catalog Number | XD96196 |
Product Name | Trifluoromethoxybenzene |
CAS | 456-55-3 |
Molecular Formula | C7H5F3O |
Molecular Weight | 162.11 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
Trifluoromethoxybenzene, also known as 1-(trifluoromethoxy)benzene or C6H5OCF3, is an organic compound with a trifluoromethoxy group (-OCF3) attached to a benzene ring. This compound possesses several notable effects and potential applications.One effect of trifluoromethoxybenzene is its unique electron-withdrawing nature. The trifluoromethoxy group withdraws electron density from the benzene ring, making the compound more reactive and potentially capable of participating in a variety of synthetic transformations. This property makes trifluoromethoxybenzene a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.The trifluoromethoxy group also imparts significant lipophilicity to trifluoromethoxybenzene. This means that the compound has a high affinity for non-polar solvents and can readily dissolve in oil-based media. This property is exploited in the development of certain industrial products like solvents, lubricants, and surfactants.Furthermore, the presence of the trifluoromethoxy group in trifluoromethoxybenzene can impart enhanced metabolic stability to the compound. This metabolic stability can contribute to increased bioavailability and longer half-life of pharmaceuticals, which is highly desirable in drug development. In addition, the trifluoromethoxy group can also influence the physicochemical properties of pharmaceuticals, potentially improving their solubility, permeability, or binding affinity.The trifluoromethoxybenzene molecule is also of interest due to its potential application in the field of fluorine chemistry. The trifluoromethoxy group is a valuable source of trifluoromethyl (CF3) moieties in synthetic transformations, offering the ability to introduce fluorine atoms into target molecules. This capacity for selective fluorination is crucial in medicinal chemistry for the discovery and development of novel drugs.Moreover, the trifluoromethoxy group in trifluoromethoxybenzene can exert a significant influence on the physical properties of a compound. The introduction of the trifluoromethoxy group can alter factors such as boiling point, melting point, and volatility, making this compound particularly valuable as a component in the development of specialty materials or additives - such as coatings or polymer modifiers.In summary, trifluoromethoxybenzene possesses several interesting effects and potential applications due to the presence of its trifluoromethoxy group. Its electron-withdrawing nature, lipophilicity, metabolic stability, fluorination capabilities, and ability to modify physical properties make it a versatile compound in organic synthesis, drug discovery, fluorine chemistry, and materials science. Understanding and utilizing these effects enable researchers to design and develop innovative compounds and materials with enhanced properties and activities.