Organic chemistry is the foundation of numerous scientific and industrial advancements, from novel materials to life-saving pharmaceuticals. Central to this field is the ability to synthesize complex molecules with precision and efficiency. Boronic acids, a class of organoboron compounds, have emerged as indispensable tools in modern synthetic organic chemistry, particularly due to their participation in palladium-catalyzed cross-coupling reactions. Among these versatile reagents, Triphenylen-2-ylboronic acid (CAS 654664-63-8) stands out for its unique structural attributes and broad applicability.

Triphenylen-2-ylboronic acid, identified by its CAS number 654664-63-8, is a solid compound, typically appearing as a white powder, with a molecular formula of C18H13BO2 and a molecular weight of 272.11 g/mol. Its defining feature is the presence of a boronic acid group (-B(OH)2) attached to a triphenylene core. This triphenylene moiety, a polycyclic aromatic hydrocarbon with a distinctive planar structure, imparts specific electronic and steric properties to the molecule. The boronic acid functionality is the key to its reactivity, making it an excellent substrate for a variety of cross-coupling reactions, most notably the Suzuki-Miyaura coupling. This reaction facilitates the formation of carbon-carbon bonds between the boronic acid and organohalides or pseudohalides, enabling chemists to construct complex aromatic and heteroaromatic systems.

The utility of Triphenylen-2-ylboronic acid in organic synthesis extends across several disciplines. In materials science, it is recognized as a crucial intermediate for the synthesis of organic light-emitting diode (OLED) materials. The rigid, extended pi-system of the triphenylene core can contribute to desirable electronic and optical properties in OLED molecules, such as high charge carrier mobility and luminescence efficiency. Researchers often seek to buy this compound to build sophisticated conjugated systems for advanced electronic applications. Furthermore, its structural motif makes it a valuable building block in medicinal chemistry for the synthesis of novel drug candidates. The ability to introduce the triphenylene fragment into target molecules via reliable coupling methods opens up avenues for exploring new therapeutic agents.

For chemists and researchers looking to procure Triphenylen-2-ylboronic acid, ensuring high purity and reliable supply is paramount. Impurities can interfere with sensitive coupling reactions, leading to lower yields, side products, and challenges in purification. This is why NINGBO INNO PHARMCHEM, a leading manufacturer and supplier of specialty chemicals from China, emphasizes the quality of its products. We offer Triphenylen-2-ylboronic acid with a guaranteed minimum purity of 97%, ensuring that our clients receive a consistent and high-performance reagent for their synthetic endeavors. Sourcing from a reputable manufacturer in China provides access to cost-effective solutions without compromising on quality, making it a strategic choice for R&D departments and production facilities.

The versatility of Triphenylen-2-ylboronic acid in organic chemistry makes it an attractive compound for researchers exploring new synthetic methodologies and novel molecular architectures. Its participation in Suzuki-Miyaura coupling, along with other potential cross-coupling reactions, allows for the modular assembly of complex organic frameworks. Whether your research focuses on developing next-generation electronic materials or discovering new pharmaceutical entities, incorporating this boronic acid derivative into your synthetic strategy can prove highly beneficial. We encourage professionals to consider NINGBO INNO PHARMCHEM as their trusted supplier for this critical organic intermediate. Contact us today to discuss how our Triphenylen-2-ylboronic acid can support your next groundbreaking synthesis.