1-bromo-4-(trifluoromethyl)-benzen CAS:402-43-7
Catalog Number | XD96195 |
Product Name | 1-bromo-4-(trifluoromethyl)-benzen |
CAS | 402-43-7 |
Molecular Formula | C7H4BrF3 |
Molecular Weight | 225.01 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
1-Bromo-4-(trifluoromethyl)-benzene is an organic compound with a molecular structure consisting of a benzene ring attached to a trifluoromethyl group and a bromine atom. This compound possesses several notable effects and potential applications.One effect of 1-Bromo-4-(trifluoromethyl)-benzene is its ability to act as a versatile building block in organic synthesis. The presence of the bromine atom and trifluoromethyl group provides reactive sites for introducing functional groups or creating new bonds. Chemists can exploit these reactive positions to modify the compound, yielding a wide range of derivatives with varying properties and applications.The trifluoromethyl group in 1-Bromo-4-(trifluoromethyl)-benzene contributes to another notable effect—the electron-withdrawing capability. This group withdraws electron density from the benzene ring, which can affect the reactivity and stability of the molecule. The electron-withdrawing nature of the trifluoromethyl group makes it particularly valuable in certain reactions where electron-poor reagents are desired or when stabilizing reactive species.Moreover, the trifluoromethyl group attached to the benzene ring imparts unique physicochemical properties to 1-Bromo-4-(trifluoromethyl)-benzene. The trifluoromethyl group is highly lipophilic, meaning it has a strong affinity for non-polar solvents and hydrophobic regions of molecules. This property can be advantageous in various applications, including the design of drugs and pesticides where enhanced membrane permeability is desired.Additionally, the trifluoromethyl group is known to influence the metabolic stability of compounds. This stability can enhance the bioavailability and efficacy of pharmaceuticals, as the trifluoromethyl group alters the way the compound is metabolized in the body. such as increased lipophilicity and decreased susceptibility to enzymatic degradation.1-Bromo-4-(trifluoromethyl)-benzene also finds application in materials science. The presence of the bromine atom allows for its utilization as a brominating agent, which is useful in the synthesis of various materials, such as flame retardants or dyes. Additionally, the trifluoromethyl group's ability to modify the physicochemical properties of compounds makes it valuable for designing coatings, adhesives, or other specialty materials.In summary, 1-Bromo-4-(trifluoromethyl)-benzene exhibits multiple effects and potential applications due to its unique structure. Its reactivity as a building block, electron-withdrawing capability, unique physicochemical properties, and influence on metabolic stability make it a valuable tool in organic synthesis, pharmaceutical development, and materials science. Understanding and utilizing these effects enable researchers to design and develop innovative compounds, materials, and applications.