1210469-11-6

Basic information

• Product Name: 10-Bromo-7-phenyl-7H-benzo[c]carbazole
• Synonyms: 10-Bromo-7-phenyl-7H-benzo[c]carbazole
• CAS NO: 1210469-11-6
• Molecular Formula: C₂₂H₁₄BrN
• Molecular Weight: 372.25726
• Mol File: 1210469-11-6.mol
• Article Data: 18

Chemical Properties

• Melting Point: 137 °C
• Boiling Point: 545.2±32.0 °C(Predicted)
• Appearance: /
• Density: 1.39±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 10-Bromo-7-phenyl-7H-benzo[c]carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 10-Bromo-7-phenyl-7H-benzo[c]carbazole(1210469-11-6)
• EPA Substance Registry System: 10-Bromo-7-phenyl-7H-benzo[c]carbazole(1210469-11-6)

Safety Data

• Hazardous Substances Data: 1210469-11-6(Hazardous Substances Data)

Usage

Appearance

White to Orange to Green powder to crystal

Uses

10-Bromo-7-phenyl-7H-benzo[c]carbazole is a useful research chemical.

Upstream product

• 205-25-4 benzo[c]carbazole 
• 530-93-8 1,2,3,4-tetrahydronaphthalen-2-one 
• 5425-53-6 5,6-dihydro-7H-benzocarbazole 
• 648432-24-0 7-phenyl-7H-benzo[c]carbazole 
• 135-19-3 β-naphthol 
• 1698-16-4 10-bromo-7H-benzo[c]carbazole 
• 108-90-7 chlorobenzene 
• 589-21-9 (4-bromophenyl)hydrazine 
• 591-50-4 iodobenzene 
• 51686-78-3 2,4-dibromonitrobenzene 
• 108-86-1 bromobenzene 
• 577-19-5 2-nitrophenyl bromide 
• 5415-59-8 1-(2-nitrophenyl)naphthalene 
• 13922-41-3 1-Naphthylboronic acid 

Downstream Products

• 1210469-12-7 C₂₈H₁₈ClN 
• 1246562-39-9 (7-phenyl-7H-benzo[c]carbazol-10-yl)boronic acid 
• 1365549-01-4 10-(9H-carbazol-3-yl)-7-phenyl-7H-benzo[c]carbazole 
• 1365549-02-5 C₄₈H₃₀N₄ 
• 1426392-21-3 C₄₃H₂₈N₄ 
• 1426391-77-6 C₃₇H₂₄N₄ 
• 1403329-75-8 C₂₈H₁₈BrN 
• 1426392-81-5 C₂₈H₂₀BNO₂ 

Relevant articles and documents

Organic compound, and organic electroluminescent device and electronic device using the same

The present invention relates to an organic compound and an organic electroluminescent device and an electronic device using the same, wherein the organic compound has a structure formed by combining an indole carbazole-based planar conjugated group in a fused manner and a dibenzofuran substituted with an aryl group. The structure has higher hole mobility and higher energy transfer efficiency, and is suitable for being used as a light-emitting host material in an organic electroluminescent device. When the organic compound is used as a light emitting host material in an organic electroluminescent device, the light emitting efficiency and the service life of the device can be effectively improved, and the working voltage is reduced.

Hole transport material and organic electroluminescent device using same

The invention discloses a hole transport material and an organic electroluminescent device using the same, which relate to the technical field of organic electroluminescence. The structural formula isshown in the specification. The hole transport material not only can improve the carrier transport efficiency, but also can improve the luminous efficiency of the device. Compared with a contrast example, the prepared organic electroluminescent device has the advantages that the voltage is reduced by 25-35%, the luminous efficiency is improved by nearly one time, and the service life is greatly prolonged, so that the driving voltage of the device can be greatly reduced by the hole transport material, the consumption of electric energy is effectively reduced, the luminous efficiency is remarkably improved, and the service life of the light-emitting device is remarkably prolonged; lighting equipment and electronic display equipment prepared from the hole transport material have the effectsof high brightness, high efficiency and low voltage, screen dark spots can be effectively avoided, and the performance is more excellent.

Fused ring organic compound and mixture and organic electronic device comprising same

The invention relates to a fused ring organic compound and a mixture and organic electronic device comprising the same. The fused ring organic compound shown in a general formula (I) has excellent electron transport properties and stability, material synthesis is simple, and when a synthesized material is applied to a device host material, the luminous efficiency and stability of the device can beimproved, and the production cost of the device can be reduced. In addition, a co-host can be formed through cooperation of the fused ring organic compound with another host with a hole transport property or a bipolar property, the electroluminescent efficiency and the service life of the device can be improved further.