Description

Bis(biphenyl-4-yl)[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]amine (CAS No. 952431-30-0) is a high-purity boronate ester derivative designed for advanced research and industrial applications. With the molecular formula C₃₆H₃₄BNO₂, this compound features a central aniline core functionalized with biphenyl groups and a pinacol boronate ester moiety, making it an excellent candidate for Suzuki-Miyaura cross-coupling reactions and other organoboron chemistry. Its well-defined structure ensures consistent reactivity, while its robust stability under various conditions makes it suitable for use in organic synthesis, materials science, and pharmaceutical development. Packaged under inert conditions to maintain integrity, this product is ideal for researchers requiring precise and reliable boron-containing building blocks.

Properties

• CAS Number: 952431-30-0
• Complexity: 725
• IUPAC Name: N,N-bis(4-phenylphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
• InChI: InChI=1S/C36H34BNO2/c1-35(2)36(3,4)40-37(39-35)31-19-25-34(26-20-31)38(32-21-15-29(16-22-32)27-11-7-5-8-12-27)33-23-17-30(18-24-33)28-13-9-6-10-14-28/h5-26H,1-4H3
• InChI Key: PESBFNLGEMHNAM-UHFFFAOYSA-N
• Exact Mass: 523.2682595
• Molecular Formula: C36H34BNO2
• Molecular Weight: 523.5
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C=C2)N(C3=CC=C(C=C3)C4=CC=CC=C4)C5=CC=C(C=C5)C6=CC=CC=C6
• Topological: 21.7
• Monoisotopic Mass: 523.2682595
• Synonyms: 952431-30-0, Bis(biphenyl-4-yl)[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]amine, N,N-Di(4-biphenylyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, N-([1,1′-biphenyl]-4-yl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-[1,1′-biphenyl]-4-amine, 2-[4-[Di(4-biphenylyl)amino]phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, N,N-bis(4-phenylphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, PESBFNLGEMHNAM-UHFFFAOYSA-N, MFCD29089353, SCHEMBL2761473, XH1440, BS-51360, DB-130327, CS-0176977, D4886, T71493, 4-[Di(4-biphenylyl)amino]phenylboronic Acid Pinacol Ester, bis(biphenyl-4-yl)-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]amine, bisbiphenyl-4-yl-[4-(4,4,5,5-tetramethyl-1,3,2-dioxa-borolan-2-yl)phenyl]amine, bisbiphenyl-4-yl-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]amine, N-(biphenyl-4-yl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)biphenyl-4-amine

Application

This compound is widely used as a key intermediate in the synthesis of organic electronic materials, such as OLEDs and OFETs, due to its electron-rich aromatic system and boronate functionality. It serves as a versatile precursor in cross-coupling reactions for constructing complex conjugated systems. Researchers also employ it in the development of advanced polymers and small-molecule semiconductors for optoelectronic applications.

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