((2-Fluoro-6-(methoxymethoxy)-8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-1-yl)ethynyl)triisopropylsilane
97%
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and advanced materials. The triisopropylsilyl-protected alkyne moiety provides stability and selectivity during synthetic processes, allowing for controlled functionalization. This chemical is often employed in the development of novel drug candidates and organic electronic materials, where precise molecular architecture is critical. Its unique structure also makes it suitable for applications in material science, such as the synthesis of conjugated polymers for optoelectronic devices.
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