For chemists engaged in organic synthesis, the availability of versatile and reactive building blocks is essential for tackling complex molecular targets. 2-Benzofuranboronic Acid (CAS: 98437-24-2) is a prime example of such a compound, offering a unique combination of the benzofuran heterocyclic system and the highly reactive boronic acid moiety. This makes it a preferred choice for a multitude of synthetic transformations.

The primary utility of 2-Benzofuranboronic Acid in organic synthesis stems from its role as a coupling partner in palladium-catalyzed cross-coupling reactions, most notably the Suzuki-Miyaura reaction. This powerful methodology enables the efficient formation of C-C bonds, allowing chemists to precisely assemble complex organic architectures. Whether for pharmaceutical intermediates, agrochemicals, or advanced materials, the ability to buy high-purity 2-Benzofuranboronic Acid from reliable manufacturers is critical for consistent results.

When procurement managers and research scientists seek to purchase this intermediate, they often look for suppliers in China, known for their robust fine chemical manufacturing capabilities. These manufacturers can typically offer 2-Benzofuranboronic Acid at competitive prices while maintaining strict quality control, ensuring a minimum purity of 97%. Access to reliable technical data, such as product specifications and safety information, further supports its effective use in synthesis labs.

The benzofuran unit itself is a common structural feature in many natural products and pharmaceuticals, underscoring the importance of efficient methods for its functionalization. 2-Benzofuranboronic Acid provides a direct route to introduce this moiety into larger, more complex molecules. For researchers and manufacturing companies, securing a stable supply chain for this intermediate is key to maintaining project timelines and ensuring production scalability. Companies that offer samples and detailed product information are invaluable partners in this endeavor.