2-Bromobenzotrifluoride CAS:392-83-6
Catalog Number | XD96194 |
Product Name | 2-Bromobenzotrifluoride |
CAS | 392-83-6 |
Molecular Formula | C7H4BrF3 |
Molecular Weight | 225.01 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
2-Bromobenzotrifluoride is an organic compound that consists of a benzene ring with a trifluoromethyl group attached at one position and a bromine atom attached at another position. This unique molecular structure gives rise to several interesting effects and potential applications.One effect of 2-Bromobenzotrifluoride is its high reactivity. The bromine atom attached to the benzene ring is an electrophilic site, making it susceptible to nucleophilic attack. This reactivity makes 2-Bromobenzotrifluoride useful as a starting material in organic synthesis. It can react with a wide range of nucleophiles, such as amines or organometallic reagents, to form new bonds and create more complex organic molecules.Another effect of 2-Bromobenzotrifluoride is its ability to act as a strong electron-withdrawing group. The trifluoromethyl group attached to the benzene ring is highly electron-withdrawing, which can have a significant impact on the reactivity and chemical behavior of the compound. This property makes 2-Bromobenzotrifluoride valuable in reactions involving electron-rich substrates. It can enhance the stability and reactivity of these substrates by withdrawing electron density from them.Furthermore, 2-Bromobenzotrifluoride can act as a precursor for the introduction of the trifluoromethyl group into other organic compounds. The trifluoromethyl group is a common motif in many pharmaceuticals and agrochemicals due to its desirable properties, such as increased lipophilicity, bioavailability, and metabolic stability. By utilizing 2-Bromobenzotrifluoride as a starting material, chemists can selectively introduce the trifluoromethyl group into target molecules, thus enhancing their pharmacological or agricultural activity.Additionally, the trifluoromethyl group in 2-Bromobenzotrifluoride can also contribute to the stability and volatility of the compound. The trifluoromethyl group is highly stable and has a low boiling point, making 2-Bromobenzotrifluoride volatile. This volatility can be advantageous in various applications, such as in the production of specialty chemicals or in the formulation of coatings or adhesives.In summary, 2-Bromobenzotrifluoride exhibits several effects and potential applications due to its unique structure. Its reactivity, electron-withdrawing capability, and ability to introduce the trifluoromethyl group make it valuable in organic synthesis, pharmaceutical development, and other related fields. Understanding and harnessing these effects allow chemists and researchers to design and create new compounds and materials with desired properties and functionalities.