1-BroMo-N-phenylcarbazole
1333002-37-1
>99%
light white powder
Handan City,Hebei Province, China
Hebei Huaqing Optoelectronics focuses on the research and production of OLED materials.
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*The following content is generated by AI and is for reference only.
1-Bromo-N-phenylcarbazole is a specialized organic intermediate widely utilized in the fields of pharmaceutical synthesis, agrochemicals, and advanced materials science. Chemically defined by the molecular formula C18H12BrN, this compound features a bromine atom substituted at the first position of the carbazole ring system, which is further N-substituted with a phenyl group. The presence of the bromine moiety renders the molecule highly reactive towards transition metal-catalyzed cross-coupling reactions, such as Suzuki-Miyaura, Stille, and Buchwald-Hartwig couplings. These reactions are pivotal for constructing complex biaryl structures that serve as core scaffolds for various bioactive molecules and functional polymers.
In the pharmaceutical industry, 1-bromo-N-phenylcarbazole acts as a crucial building block for synthesizing novel kinase inhibitors and anti-inflammatory agents. Its rigid carbazole backbone contributes to specific binding affinities within biological targets, while the bromine handle allows for precise structural diversification. Furthermore, in the realm of optoelectronics, derivatives of this compound are investigated for use in organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs). The extended pi-conjugation system facilitates efficient charge transport and tunable emission properties, making it valuable for next-generation display technologies and photovoltaic cells.
The standard catalog number for this substance often includes CAS Registry Number 39746-50-4, ensuring traceability and purity verification across global supply chains. It typically appears as a pale yellow to off-white crystalline powder, stable under standard storage conditions but sensitive to strong oxidizing agents. Researchers prioritize high-purity grades to prevent side reactions during multi-step syntheses. Due to its versatility in forming carbon-carbon and carbon-heteroatom bonds, 1-bromo-N-phenylcarbazole remains an indispensable reagent in modern medicinal chemistry laboratories and industrial R&D departments focused on developing high-performance electronic materials. Its unique structural characteristics continue to drive innovation in creating safer drugs and more efficient energy devices.