1246562-40-2

Basic information

• Product Name: N-[1,1'-biphenyl]-4-yl-N-(4-broMophenyl)-9,9-diMethyl-9H-Fluoren-2-aMine
• Synonyms: N-[1,1'-biphenyl]-4-yl-N-(4-broMophenyl)-9,9-diMethyl-9H-Fluoren-2-aMine;N-(biphenyl-4-yl)-N-(4-broMophenyl)-9,9-diMethyl-9;2-Amino-N-[(1,1'-biphenyl)-4-yl]-N-(4-bromophenyl)-9,9-dimethylfluorene;2-Amino-N-[(1,1'-biphenyl)-4-yl]-N-(4-bromophenyl)-9,9-dimethylfluorene;1'-biphenyl]-4-yl-N-(4-broMophenyl)-9;9-diMethyl-9H-Fluoren-2-aMine;N-BP-FL-PBr
• CAS NO: 1246562-40-2
• Molecular Formula: C₃₃H₂₆BrN
• Molecular Weight: 516.47024
• Mol File: 1246562-40-2.mol
• Article Data: 33

Chemical Properties

• Melting Point: 159.0 to 163.0 °C
• Boiling Point: 655.9±55.0 °C(Predicted)
• Appearance: /
• Density: 1.293±0.06 g/cm3 (20 oC 760 Torr), Calc.*
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• Solubility: soluble in Tetrahydrofuran
• PKA: -3.55±0.40(Predicted)
• CAS DataBase Reference: N-[1,1'-biphenyl]-4-yl-N-(4-broMophenyl)-9,9-diMethyl-9H-Fluoren-2-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[1,1'-biphenyl]-4-yl-N-(4-broMophenyl)-9,9-diMethyl-9H-Fluoren-2-aMine(1246562-40-2)
• EPA Substance Registry System: N-[1,1'-biphenyl]-4-yl-N-(4-broMophenyl)-9,9-diMethyl-9H-Fluoren-2-aMine(1246562-40-2)

Safety Data

• Hazardous Substances Data: 1246562-40-2(Hazardous Substances Data)

Usage

Description

N-[1,1'-biphenyl]-4-yl-N-(4-bromophenyl)-9,9-dimethyl-9H-Fluoren-2-amine is a complex organic compound characterized by its unique molecular structure, which features a biphenyl and bromophenyl group attached to a fluorenylamine core. N-[1,1'-biphenyl]-4-yl-N-(4-bromophenyl)-9,9-dimethyl-9H-Fluoren-2-amine is known for its potential applications in the development of advanced materials and devices.

Uses

Used in Organic Synthesis:
N-[1,1'-biphenyl]-4-yl-N-(4-bromophenyl)-9,9-dimethyl-9H-Fluoren-2-amine is used as a reactant in the synthesis of novel hole transport materials for efficient green electroluminescent devices. Its unique structure allows for the creation of materials with enhanced charge transport properties, which are crucial for the performance of electroluminescent devices.
Used in Optoelectronics Industry:
In the optoelectronics industry, N-[1,1'-biphenyl]-4-yl-N-(4-bromophenyl)-9,9-dimethyl-9H-Fluoren-2-amine is used as a key component in the development of green electroluminescent devices. Its incorporation into these devices contributes to improved energy efficiency and color quality, making it a valuable asset in the design and manufacture of next-generation optoelectronic products.
Used in Research and Development:
N-[1,1'-biphenyl]-4-yl-N-(4-bromophenyl)-9,9-dimethyl-9H-Fluoren-2-amine is also utilized in research and development settings, where it serves as a starting material for the exploration of new chemical reactions and the synthesis of innovative materials. Its unique properties make it an attractive candidate for further study and potential applications in various fields.

Upstream product

• 897671-69-1 N?(biphenyl?4?yl)?9,9?dimethyl?9H?fluorene?2?amine 
• 108-86-1 bromobenzene 
• 92-67-1 4-phenylalanine 
• 1326137-97-6 N-([1,1′-biphenyl]-4-yl)-9,9′-dimethyl-9H-fluoren-3-amine 
• 106-37-6 1.4-dibromobenzene 
• 589-87-7 1,4-bromoiodobenzene 

Downstream Products

• 1242056-42-3 N-(1,1‘-biphenyl-4-yl)-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]-9,9-dimethyl-9H-fluoren-2-amine 
• 1347758-80-8 (N-[1,1‘-biphenyl]-4-yl)-9,9-dimethyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl)phenyl)-9H-fluorene-2-amine 

Relevant articles and documents

Novel organic dye sensitizers containing fluorenyl and biphenyl moieties for solar cells

Three novel triarylamine dyes (AFL1–AFL3) containing fluorenyl and the biphenyl moieties have been designed and synthesized for application in dye-sensitized solar cells. The light-harvesting capabilities and photovoltaic performance of these dyes were investigated systematically through comparison of different π-bridges. The dye with a furan linker exhibited a higher open-circuit voltage (VOC) and monochromatic incident photon-to-current conversion efficiency (IPCE) compared to thiophene and benzene linker. Thus, AFL3 containing a furan linker exhibited the maximum overall conversion efficiency of 5.81% (VOC?=?760?mV,?JSC?=?11.36?mA?cm?2and ff?=?0.68) under standard global AM 1.5 G solar condition.

Organic electroluminescent material and device thereof

An organic electroluminescent material and a device thereof are disclosed. The organic electroluminescent material is a monoamine aromatic compound containing a dibenzo selenophen structure. The compound can be used as an organic layer material such as a hole transport material and an electron blocking material in an organic electroluminescent device. By using the compound, the characteristics ofheat resistance, driving voltage, luminous efficiency, service lifetime and the like of the OLED device can be effectively improved.

Organic electroluminescent compounds and organic electroluminescent device using the same

The present invention relates to an organic electroluminescent compound applied to a hole transfer material, which is characterized by being presented by chemical formula 1-1 and chemical formula 1-2. The organic electroluminescent compound according to the present invention can manufacture an organic electroluminescent device having improved light emitting efficiency and life properties, when applied to a hole transfer layer of the organic electroluminescent device.