The Suzuki-Miyaura cross-coupling reaction has revolutionized organic synthesis, offering a powerful and versatile method for forming carbon-carbon bonds. At the heart of this reaction are boronic acids and their esters, which act as nucleophilic coupling partners. Among these crucial reagents, N,N-Diphenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (CAS: 267221-88-5) stands out as a valuable and often sought-after component.

This compound, characterized by its diphenylamine functional group and the stable pinacol boronate ester moiety, is an excellent substrate for Suzuki-Miyaura coupling. The presence of the electron-rich diphenylamine group can influence the electronic properties of the resulting coupled products, making it particularly useful in the synthesis of advanced materials like those used in organic electronics. Researchers and scientists frequently search for this specific boronic ester to create novel conjugated systems for applications such as OLEDs, organic photovoltaics, and chemosensors.

As a leading manufacturer and supplier of fine chemical intermediates, we are proud to offer N,N-Diphenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline to the global market. Our commitment to quality ensures that we supply this compound at high purity levels, crucial for the success of sensitive cross-coupling reactions. When you decide to buy this reactant, you are investing in the precision and efficiency of your synthesis.

For procurement managers and laboratory chemists looking for a reliable source to purchase N,N-Diphenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, our services are designed to meet your needs. We provide competitive pricing, consistent quality, and responsive customer support. If your research or production involves Suzuki-Miyaura coupling and requires this specific boronic ester, we encourage you to contact us for a quotation and to learn more about our supply capabilities from China.