Description
11-([1,1′-Biphenyl]-3-yl)-11,12-dihydroindolo[2,3-a]carbazole (CAS No. 1449754-80-6) is a high-purity organic compound with the molecular formula C30H20N2. This indolo[2,3-a]carbazole derivative features a biphenyl substitution at the 11-position, making it a valuable building block for advanced materials research. The compound’s extended π-conjugated system and rigid planar structure make it particularly interesting for applications in organic electronics and optoelectronics.
Our product is synthesized under严格控制的条件 to ensure exceptional purity (>98%) and batch-to-batch consistency. It is supplied as a fine yellow to orange powder with excellent solubility in common organic solvents such as dichloromethane, tetrahydrofuran, and dimethylformamide. Each batch undergoes rigorous quality control including HPLC, NMR, and mass spectrometry analysis.
This specialty chemical is ideal for researchers developing organic semiconductors, OLED materials, or photoconductive compounds. The compound’s unique electronic properties and thermal stability make it particularly suitable for use in hole-transport materials and host materials in phosphorescent OLED devices.
Properties
- CAS Number: 1449754-80-6
- Complexity: 655
- IUPAC Name: 12-(3-phenylphenyl)-11H-indolo[2,3-a]carbazole
- InChI: InChI=1S/C30H20N2/c1-2-9-20(10-3-1)21-11-8-12-22(19-21)32-28-16-7-5-14-24(28)26-18-17-25-23-13-4-6-15-27(23)31-29(25)30(26)32/h1-19,31H
- InChI Key: KXDSITDVSDFQIY-UHFFFAOYSA-N
- Exact Mass: 408.162648646
- Molecular Formula: C30H20N2
- Molecular Weight: 408.5
- SMILES: C1=CC=C(C=C1)C2=CC(=CC=C2)N3C4=CC=CC=C4C5=C3C6=C(C=C5)C7=CC=CC=C7N6
- Topological: 20.7
- Monoisotopic Mass: 408.162648646
- Synonyms: 1449754-80-6, 11-([1,1′-Biphenyl]-3-yl)-11,12-dihydroindolo[2,3-a]carbazole, 11-[1,1′-Biphenyl]-3-yl-11,12-dihydro-indolo[2,3-a]carbazole, 12-(3-phenylphenyl)-11H-indolo[2,3-a]carbazole, 11-(biphenyl-3-yl)-11,12-dihydroindolo[2,3-a]carbazole, SCHEMBL22355457, MFCD32703956, BS-46055, CS-0162872, D80596
Application
This compound serves as a key intermediate in the synthesis of advanced organic electronic materials. Researchers utilize it in the development of high-performance organic light-emitting diodes (OLEDs) due to its excellent hole-transport properties. The material shows promise in photovoltaic applications as a donor material in organic solar cells. Its rigid conjugated structure makes it suitable for studying charge transport mechanisms in organic semiconductors.
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