Description

9-([1,1′-Biphenyl]-4-yl)-9′-phenyl-9H,9’H-3,3′-bicarbazole (CAS No. 1454567-05-5) is a high-purity organic compound with the molecular formula C₄₂H₂₈N₂. This advanced bicarbazole derivative features a rigid, conjugated structure, making it an excellent candidate for optoelectronic applications. The compound is synthesized under stringent conditions to ensure >98% purity, as verified by HPLC and NMR spectroscopy. Its IUPAC name, 3-(9-phenylcarbazol-3-yl)-9-(4-phenylphenyl)carbazole, reflects its precise molecular architecture. Packaged in amber glass vials under inert atmosphere to prevent degradation, this product is ideal for researchers developing OLEDs, photovoltaics, or other organic semiconductor devices. Each batch is supplied with comprehensive analytical data including mass spectrometry and elemental analysis results.

Properties

• CAS Number: 1454567-05-5
• Complexity: 941
• IUPAC Name: 3-(9-phenylcarbazol-3-yl)-9-(4-phenylphenyl)carbazole
• InChI: InChI=1S/C42H28N2/c1-3-11-29(12-4-1)30-19-23-34(24-20-30)44-40-18-10-8-16-36(40)38-28-32(22-26-42(38)44)31-21-25-41-37(27-31)35-15-7-9-17-39(35)43(41)33-13-5-2-6-14-33/h1-28H
• InChI Key: PFCJGRHBQVDYQK-UHFFFAOYSA-N
• Exact Mass: 560.225248902
• Molecular Formula: C42H28N2
• Molecular Weight: 560.7
• SMILES: C1=CC=C(C=C1)C2=CC=C(C=C2)N3C4=C(C=C(C=C4)C5=CC6=C(C=C5)N(C7=CC=CC=C76)C8=CC=CC=C8)C9=CC=CC=C93
• Topological: 9.9
• Monoisotopic Mass: 560.225248902
• Synonyms: 1454567-05-5, 9-([1,1′-Biphenyl]-4-yl)-9′-phenyl-9H,9’H-3,3′-bicarbazole, 9-[1,1′-Biphenyl]-4-yl-9′-phenyl-3,3′-bicarbazole, 9-(4-Biphenylyl)-9′-phenyl-9H,9’H-3,3′-bicarbazole, 9-[1,1′-Biphenyl]-4-yl-9′-phenyl-3,3′-bi-9H-carbazole, MFCD31735647, 9-(4-BIPHENYLYL)-9-PHENYL-9H,9H-3,3-BICARBAZOLE, 9-(4-Biphenylyl)-9 inverted exclamation mark -phenyl-9H,9 inverted exclamation mark H-3,3 inverted exclamation mark -bicarbazole, SCHEMBL15502589, AC4326, BS-44406, SY247602, DB-415617, CS-0188144, 3-(9-phenylcarbazol-3-yl)-9-(4-phenylphenyl)carbazole

Application

This bicarbazole derivative serves as a high-performance hole transport material in organic light-emitting diodes (OLEDs) due to its excellent charge carrier mobility. Researchers utilize it as an emissive layer component in blue-phosphorescent OLED devices owing to its wide bandgap and triplet energy properties. The compound also shows promise in perovskite solar cells as a passivation layer to enhance device stability and efficiency.

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