(1H-Pyrrolo[2,3-c]pyridin-4-yl)boronic acid, commonly referred to as $name$, is a versatile compound utilized in various chemical synthesis processes. Its unique structure provides a valuable building block for the creation of complex molecules and compounds across different industries.In chemical synthesis, (1H-Pyrrolo[2,3-c]pyridin-4-yl)boronic acid serves as a crucial reagent for the formation of carbon-carbon and carbon-heteroatom bonds. Its boronic acid functional group enables it to participate in Suzuki-Miyaura cross-coupling reactions, allowing for the selective construction of biaryl compounds. This reaction, catalyzed by palladium, has become a fundamental transformation in organic chemistry and is widely employed in the synthesis of pharmaceuticals, agrochemicals, and materials science.Furthermore, the presence of the pyrrolopyridine scaffold in (1H-Pyrrolo[2,3-c]pyridin-4-yl)boronic acid offers opportunities for further derivatization and structural modification. This flexibility facilitates the development of novel molecules with diverse properties and functionalities. By incorporating (1H-Pyrrolo[2,3-c]pyridin-4-yl)boronic acid into synthetic routes, chemists can access a wide range of structurally complex and biologically active compounds for various applications.Overall, the utility of (1H-Pyrrolo[2,3-c]pyridin-4-yl)boronic acid in chemical synthesis lies in its ability to enable the efficient construction of intricate molecular frameworks and the synthesis of valuable intermediates for the pharmaceutical, agrochemical, and materials industries.
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