1884420-79-4 Usage
Uses
Used in Organic Light-Emitting Diodes (OLEDs):
2,7-bis(4-bromophenyl)-N-hexylcarbazole is used as a material in OLEDs for its high thermal stability and good charge transport properties. These characteristics are essential for the creation of efficient and durable light-emitting devices.
Used in Organic Photovoltaic (OPV) Devices:
In the field of organic photovoltaics, 2,7-bis(4-bromophenyl)-N-hexylcarbazole serves as a component that contributes to the efficiency and performance of OPV devices, leveraging its electron-donating properties and charge transport capabilities.
Used in Organic Electronic Applications:
2,7-bis(4-bromophenyl)-N-hexylcarbazole is utilized in various organic electronic applications due to its unique molecular structure and electron-donating properties, which make it a promising candidate for the development of advanced optoelectronic devices.
Used in Research for Optoelectronic Devices:
2,7-bis(4-bromophenyl)-N-hexylcarbazole is also a subject of research for its potential use in optoelectronic devices, where its properties are explored to enhance the performance and capabilities of next-generation electronic systems.
Check Digit Verification of cas no
The CAS Registry Mumber 1884420-79-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,8,4,4,2 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1884420-79:
(9*1)+(8*8)+(7*8)+(6*4)+(5*4)+(4*2)+(3*0)+(2*7)+(1*9)=204
204 % 10 = 4
So 1884420-79-4 is a valid CAS Registry Number.
1884420-79-4Relevant articles and documents
N,N'-diphenyl-N,N'-di(9,9-dimethyl fluorene-2-yl)-N-hexyl-(4,4'-diamine phenyl) carbazole and synthetic method thereof
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Paragraph 0009; 0028; 0029, (2016/10/08)
The invention discloses N,N'-diphenyl-N,N'-di(9,9-dimethyl fluorene-2-yl)-N-hexyl-(4,4'-diamine phenyl) carbazole and a synthetic method thereof and belongs to the field of organic synthesis. According to the synthetic method, 2,7-dibromo-carbazole is used as a raw material and subjected to N-alkylation and a Suzuki coupled reaction to synthesize 2,7-di(4-bromophenyl)-N-hexyl carbazole; 2-bromo-9,9-dimethyl fluorene and aniline are used as raw materials and subjected to a Buchwald-Hartwig coupled reaction to synthesize 9,9-dimethyl-N-phenyl fluorine-2-amine; lastly, 2,7-di(4-bromophenyl)-N-hexyl carbazole and the 9,9-dimethyl-N-phenyl fluorine-2-amine are used as raw materials and subjected to a Buchwald-Hartwig coupled reaction to synthesize a target compound. The target compound has good heat stability and glass transition temperature and is suitable for hole transport materials of organic light-emitting devices.
