Description

(4-(9-Phenyl-9H-carbazol-3-yl)phenyl)boronic acid (CAS: 1240963-55-6) is a high-purity boronic acid derivative featuring a carbazole-phenyl hybrid structure, designed for advanced research and industrial applications. With the molecular formula C₂₄H₁₈BNO₂, this compound exhibits excellent stability and reactivity, making it a valuable building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its unique aromatic system enhances electronic properties, ideal for materials science, OLED development, and pharmaceutical research. Each batch undergoes rigorous QC testing (HPLC, NMR) to ensure ≥95% purity, meeting the stringent demands of researchers and scientists. Packaged under inert gas to prevent degradation.

Properties

• CAS Number: 1240963-55-6
• Complexity: 515
• IUPAC Name: [4-(9-phenylcarbazol-3-yl)phenyl]boronic acid
• InChI: InChI=1S/C24H18BNO2/c27-25(28)19-13-10-17(11-14-19)18-12-15-24-22(16-18)21-8-4-5-9-23(21)26(24)20-6-2-1-3-7-20/h1-16,27-28H
• InChI Key: CFZRUXMJHALVPF-UHFFFAOYSA-N
• Exact Mass: 363.1430590
• Molecular Formula: C24H18BNO2
• Molecular Weight: 363.2
• SMILES: B(C1=CC=C(C=C1)C2=CC3=C(C=C2)N(C4=CC=CC=C43)C5=CC=CC=C5)(O)O
• Topological: 45.4
• Monoisotopic Mass: 363.1430590
• Synonyms: 1240963-55-6, (4-(9-Phenyl-9H-carbazol-3-yl)phenyl)boronic acid, Boronic acid, B-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]-, [4-(9-phenylcarbazol-3-yl)phenyl]boronic acid, [4-(9-phenyl-9H-carbazol-3-yl)phenyl]boronic acid, B-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]-Boronic acid, MFCD30063200, 4-(9-Phenyl-9H-carbazol-3-yl)phenylboronic acid, SCHEMBL854107, C24H18BNO2, CFZRUXMJHALVPF-UHFFFAOYSA-N, AKOS027384010, DS-13443, DB-108422, CS-0156116, F18763, (4-(9-Phenyl-9H-carbazol-3-yl)phenyl)boronicacid, B-[4-(9-Phenyl-9H-carbazol-3-yl)phenyl]-boronicacid

Application

This boronic acid derivative is widely used in organic electronics as a key intermediate for synthesizing conjugated polymers and small molecules for OLEDs and photovoltaic devices. It serves as a versatile coupling partner in palladium-catalyzed cross-coupling reactions to create complex biaryl structures. Researchers also employ it in drug discovery for developing kinase inhibitors and boron-containing therapeutics.

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