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Atomfair 9-Phenyl-3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole C30H28BNO2

Description 9-Phenyl-3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole (CAS No. 1569294-77-4) is a high-purity boronate ester derivative of carbazole, designed for advanced research and synthetic applications. With the molecular formula C30H28BNO2, this compound features a carbazole core functionalized with a phenyl group at the 9-position and a pinacol boronate ester at the 3-position, making it a versatile intermediate for Suzuki-Miyaura cross-coupling reactions. Its rigid aromatic structure and boron-containing moiety enable precise modifications in organic electronic materials, OLEDs, and pharmaceutical scaffolds. This product is rigorously tested for purity and stability, ensuring optimal performance in demanding laboratory conditions. Available in various quantities, it is ideal for researchers seeking…

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Description

Description

9-Phenyl-3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole (CAS No. 1569294-77-4) is a high-purity boronate ester derivative of carbazole, designed for advanced research and synthetic applications. With the molecular formula C30H28BNO2, this compound features a carbazole core functionalized with a phenyl group at the 9-position and a pinacol boronate ester at the 3-position, making it a versatile intermediate for Suzuki-Miyaura cross-coupling reactions. Its rigid aromatic structure and boron-containing moiety enable precise modifications in organic electronic materials, OLEDs, and pharmaceutical scaffolds. This product is rigorously tested for purity and stability, ensuring optimal performance in demanding laboratory conditions. Available in various quantities, it is ideal for researchers seeking reliable building blocks for complex molecular architectures.

  • CAS No: 1569294-77-4
  • Molecular Formula: C30H28BNO2
  • Molecular Weight: 445.4
  • Exact Mass: 445.2213093
  • Monoisotopic Mass: 445.2213093
  • IUPAC Name: 9-phenyl-3-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbazole
  • SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC(=CC=C2)C3=CC4=C(C=C3)N(C5=CC=CC=C54)C6=CC=CC=C6
  • Synonyms: 9-Phenyl-3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole, 1569294-77-4, SCHEMBL12415382, MFCD32670128, G67981

Application

This compound serves as a key intermediate in the synthesis of organic semiconductors and light-emitting materials for OLED applications. Its boronate ester group facilitates efficient cross-coupling reactions, enabling the construction of extended ??-conjugated systems. Researchers also utilize it in the development of pharmaceutical candidates due to its carbazole scaffold, known for bioactive properties. Additionally, it is employed in materials science for designing advanced polymers with tailored optoelectronic characteristics.

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