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

Description

10-Bromo-7-phenyl-7H-benzo[c]carbazole is a synthetic organic compound characterized by its unique molecular structure, featuring a benzo[c]carbazole core with a bromine atom at the 10th position and a phenyl group at the 7th position. It exhibits a variable appearance, ranging from white to orange to green powder or crystalline form, depending on the synthesis method and purity.

Uses

Used in Research and Development:
10-Bromo-7-phenyl-7H-benzo[c]carbazole is utilized as a valuable research chemical, particularly in the fields of organic chemistry, medicinal chemistry, and materials science. Its unique structure and properties make it a promising candidate for the development of new compounds and materials with potential applications in various industries.
Used in Organic Chemistry:
In the realm of organic chemistry, 10-Bromo-7-phenyl-7H-benzo[c]carbazole serves as a versatile intermediate for the synthesis of more complex organic molecules. Its bromine atom and phenyl group can be further functionalized or modified to create a wide range of derivatives with diverse chemical properties and potential applications.
Used in Medicinal Chemistry:
10-Bromo-7-phenyl-7H-benzo[c]carbazole is employed as a key building block in the design and synthesis of novel pharmaceutical agents. Its unique structure and chemical properties can be harnessed to develop new drugs with improved efficacy, selectivity, and safety profiles for the treatment of various diseases and medical conditions.
Used in Materials Science:
In materials science, 10-Bromo-7-phenyl-7H-benzo[c]carbazole can be used as a component in the development of advanced materials with specific properties, such as organic semiconductors, optoelectronic materials, and functional coatings. Its incorporation into these materials can lead to enhanced performance and new functionalities.
Overall, 10-Bromo-7-phenyl-7H-benzo[c]carbazole is a versatile and valuable research chemical with a wide range of potential applications across various scientific disciplines and industries. Its unique structure and properties make it an attractive candidate for further exploration and development.

Upstream product

• 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 
• 13922-41-3 1-Naphthylboronic acid 
• 5415-59-8 1-(2-nitrophenyl)naphthalene 
• 577-19-5 2-nitrophenyl bromide 
• 51686-78-3 2,4-dibromonitrobenzene 
• 108-86-1 bromobenzene 
• 648432-24-0 7-phenyl-7H-benzo[c]carbazole 
• 5425-53-6 5,6-dihydro-7H-benzocarbazole 
• 530-93-8 1,2,3,4-tetrahydronaphthalen-2-one 
• 205-25-4 benzo[c]carbazole 

Downstream Products

• 1210469-12-7 C₂₈H₁₈ClN 
• 1356174-59-8 C₃₇H₂₈N₂ 
• 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.

ORGANIC MIXTURE AND APPLICATION THEREOF IN ORGANIC ELECTRONIC DEVICES

The present invention relates to an organic mixture and an application thereof in organic electronic devices. The organic mixture comprises a spirofluorene organic compound containing a fused heterocyclic ring and an aromatic fused heterocyclic organic compound containing an electron-donating group. A combination of the two materials may be used as a host material of a phosphorescent organic light-emitting diode (OLED), which may use the energy of excitons and balance the charge transport to the greatest extent and which may effectively reduce the concentration of excitons and the operating voltage of a corresponding device, thereby effectively improving the efficiency and service life of the related electronic device in order to provide an effective solution for improving the overall performance of an organic electronic device.

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.