The compound 2-(5-Chloro-2-methyl-4-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, also known as $name$, is a versatile reagent widely used in chemical synthesis. Its unique structure containing boron and fluorinated aromatic rings makes it a valuable tool in organic chemistry.One key application of $name$ in chemical synthesis is as a boron source in Suzuki-Miyaura cross-coupling reactions. In this reaction, $name$ acts as a boronate ester, participating in the coupling with various organic halides or pseudohalides to form biaryl compounds. The versatility of $name$ in this reaction allows for the rapid and efficient synthesis of complex organic molecules with high regio- and stereo-selectivity.Additionally, $name$ can be utilized in the formation of heterocyclic compounds through its involvement in metal-catalyzed coupling reactions. By incorporating $name$ into the synthetic pathway, chemists can access a diverse array of functionalized heterocycles, which are important building blocks in pharmaceutical and material science research.Overall, the strategic incorporation of 2-(5-Chloro-2-methyl-4-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane in chemical synthesis enables efficient access to complex organic molecules and facilitates the development of novel materials with tailored properties.
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