Description
9′-(2-Anthracenyl)-3,3”,6,6”-tetrakis(1,1-dimethylethyl)-9,3′:6′,9”-ter-9H-carbazole (CAS: 1332640-08-0) is a high-purity, synthetic carbazole derivative designed for advanced research applications. With the molecular formula C66H63N3, this compound features a rigid, multi-branched structure incorporating anthracene and tert-butyl-substituted carbazole moieties, making it an excellent candidate for organic electronic materials, photoluminescent studies, and molecular engineering. Its high thermal and oxidative stability, combined with tunable optoelectronic properties, makes it suitable for use in OLEDs, photovoltaic devices, and as a building block for supramolecular architectures. Available in milligram to gram quantities with ≥95% purity (HPLC), this product is ideal for researchers seeking specialized heterocyclic compounds for cutting-edge applications.
Properties
- CAS Number: 1332640-08-0
- Complexity: 1610
- IUPAC Name: 9-(2-anthryl)-3,6-bis(3,6-ditert-butylcarbazol-9-yl)carbazole
- InChI: InChI=1S/C66H63N3/c1-63(2,3)44-18-25-57-51(34-44)52-35-45(64(4,5)6)19-26-58(52)68(57)49-23-29-61-55(38-49)56-39-50(24-30-62(56)67(61)48-22-17-42-31-40-15-13-14-16-41(40)32-43(42)33-48)69-59-27-20-46(65(7,8)9)36-53(59)54-37-47(66(10,11)12)21-28-60(54)69/h13-39H,1-12H3
- InChI Key: UFNLNMGNPJXMRI-UHFFFAOYSA-N
- Exact Mass: 897.50219902
- Molecular Formula: C66H63N3
- Molecular Weight: 898.2
- SMILES: CC(C)(C)C1=CC2=C(C=C1)N(C3=C2C=C(C=C3)C(C)(C)C)C4=CC5=C(C=C4)N(C6=C5C=C(C=C6)N7C8=C(C=C(C=C8)C(C)(C)C)C9=C7C=CC(=C9)C(C)(C)C)C1=CC2=CC3=CC=CC=C3C=C2C=C1
- Topological: 14.8
- Monoisotopic Mass: 897.50219902
- Synonyms: 1332640-08-0, 9,3′:6′,9”-Ter-9H-carbazole, 9′-(2-anthracenyl)-3,3”,6,6”-tetrakis(1,1-dimethylethyl)-, SCHEMBL2604402, 9′-(2-Anthracenyl)-3,3”,6,6”-tetrakis(1,1-dimethylethyl)-9,3′:6′,9”-ter-9H-carbazole
Application
This carbazole-anthracene hybrid compound is primarily used in the development of organic light-emitting diodes (OLEDs) due to its efficient charge transport and luminescent properties. Researchers also employ it as a key intermediate in synthesizing advanced conjugated polymers for photovoltaic and semiconductor applications. Its rigid, sterically hindered structure makes it a candidate for studying aggregation-induced emission (AIE) phenomena in material science.
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