The (3'-Chloro-[1,1'-biphenyl]-3-yl)boronic acid, also known as $name$, is a versatile chemical compound widely utilized in organic synthesis. This compound serves as a crucial building block in the creation of various organic molecules due to its unique reactivity and properties.One key application of (3'-Chloro-[1,1'-biphenyl]-3-yl)boronic acid is in the field of Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by palladium, allows for the formation of carbon-carbon bonds between an aryl halide and an organoboron compound. The presence of the boronic acid group in $name$ enables it to participate effectively in this coupling reaction, leading to the synthesis of biaryl compounds with high efficiency and selectivity.Moreover, (3'-Chloro-[1,1'-biphenyl]-3-yl)boronic acid finds application in the construction of complex molecular structures, such as pharmaceutical intermediates, agrochemicals, and materials science. Its compatibility with various functional groups and its stability under a range of reaction conditions make it a valuable tool for chemists working in the field of organic synthesis.Overall, the (3'-Chloro-[1,1'-biphenyl]-3-yl)boronic acid, or $name$, plays a significant role in modern chemical synthesis by enabling the efficient and controlled formation of carbon-carbon bonds, facilitating the creation of diverse and valuable organic compounds.
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