205-25-4

Basic information

• Product Name: 7H-BENZO[C]CARBAZOLE
• Synonyms: 7H-BENZO[C]CARBAZOLE;3,4-Benzocarbazole;7-Aza-7H-benzo[c]fluorene;BENZO(C)CARBAZOLE
• CAS NO: 205-25-4
• Molecular Formula: C₁₆H₁₁N
• Molecular Weight: 217.27
• EINECS: 205-909-8
• Product Categories: OLED
• Mol File: 205-25-4.mol
• Article Data: 68

Chemical Properties

• Melting Point: 135-137℃
• Boiling Point: 347.82°C (rough estimate)
• Flash Point: 207.893 °C
• Appearance: /
• Density: 1.277
• Vapor Pressure: 4.5E-08mmHg at 25°C
• Refractive Index: 1.8230 (estimate)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 17.00±0.30(Predicted)
• CAS DataBase Reference: 7H-BENZO[C]CARBAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 7H-BENZO[C]CARBAZOLE(205-25-4)
• EPA Substance Registry System: 7H-BENZO[C]CARBAZOLE(205-25-4)

Safety Data

• Hazardous Substances Data: 205-25-4(Hazardous Substances Data)

Usage

General Description

7H-Benzo[c]carbazole is a chemical compound that belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three-ring system consisting of two benzene rings fused with a pyrrole ring. 7H-Benzo[c]carbazole, specifically, is characterized by its planar geometry and aromaticity. It is a polycyclic aromatic hydrocarbon, which means it has multiple interconnected aromatic rings. The compound is often used in organic chemistry as a building block for synthesizing more complex structures, including certain types of dyes and drugs. However, it can also be a health hazard as it is a possible carcinogen.

InChI:InChI=1/C16H11N/c1-2-6-12-11(5-1)9-10-15-16(12)13-7-3-4-8-14(13)17-15/h1-10,17H

Upstream product

• 97555-59-4 3-phenyl-3H-naphtho[1,2-d][1,2,3]triazole 
• 100-63-0 phenylhydrazine 
• 135-19-3 β-naphthol 
• 64-17-5 ethanol 
• 92-70-6 3-Hydroxy-2-naphthoic acid 
• 567-47-5 2-hydroxy-naphthalene-1-sulfonic acid 
• 1342878-79-8 C₂₁H₂₂N₂O₂ 
• 62-53-3 aniline 
• 98154-45-1 11b-methyl-11bH-benzocarbazole 
• 135-88-6 N-Phenyl-2-naphthylamine 
• 854161-68-5 1-(naphthalen-2-yl)-1H-benzo[d][1,2,3]triazole 
• 5425-53-6 5,6-dihydro-7H-benzocarbazole 
• 92795-22-7 2-nitro-1-phenylnaphthalene 
• 20841-53-6 Benzonaphthto<1,2-d>thiophene 7,7-dioxide 

Downstream Products

• 1262867-02-6 C₃₇H₂₄N₂ 
• 1262867-03-7 C₃₇H₂₃BrN₂ 
• 1262867-04-8 C₅₅H₃₈N₂Si 
• 1262867-01-5 C₂₅H₁₅ClN₂ 
• 1210469-11-6 10-bromo-7-phenyl-7H-benzo[c]carbazole 
• 1210469-12-7 C₂₈H₁₈ClN 
• 1210468-70-4 C₅₂H₃₆N₂ 
• 648432-24-0 7-phenyl-7H-benzo[c]carbazole 
• 1426392-21-3 C₄₃H₂₈N₄ 
• 1426391-77-6 C₃₇H₂₄N₄ 
• 1403329-75-8 C₂₈H₁₈BrN 
• 1426392-81-5 C₂₈H₂₀BNO₂ 
• 1365548-95-3 C₃₆H₂₃N₃ 
• 1415223-37-8 C₄₂H₂₆N₄ 

Relevant articles and documents

A design strategy of bipolar host materials for more than 30 times extended lifetime in phosphorescent organic light-emitting diodes using benzocarbazole and quinazoline

Stable host materials based on benzocarbazole and quinazoline were synthesized to establish a design strategy of bipolar hosts for elongated lifetime in orange phosphorescent organic light-emitting diodes (PHOLEDs). Three host materials with benzocarbazole and quinazoline connected directly or through a phenyl linker were compared in terms of the device lifetime of the orange PHOLEDs. The connection between benzocarbazole and quinazoline through a phenyl linker was an effective way of improving the lifetime of the red PHOLEDs by more than twice and the molecular orbital distribution of the hosts was well correlated with the lifetime of the PHOLEDs. In particular, the lifetime of the PHOLEDs was extended by more than 30 times compared to a conventional PHOLED with a common CBP host.

Synthesis of non-C2symmetrical NOBIN-type biaryls through a cascade N -arylation and [3,3]-sigmatropic rearrangement from O -arylhydroxylamines and diaryliodonium salts

We developed herein a regioselective construction of non-C2 symmetrical NOBIN-type biaryls through a cascade N-arylation and [3,3]-sigmatropic rearrangement from O-arylhydroxylamines and diaryliodonium salts under mild conditions. The employment of copper salt could inhibit the further O-arylation of the newly formed biaryl products, otherwise, O-arylated NOBIN-type products were furnished in moderate to good isolated yields. The products of this protocol can be further converted into highly valuable functional molecules and heterocycles.

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND A ELECTRONIC DEVICE THEREOF

The present invention relates to a novel compound, an organic electric element using the same, and an electronic device thereof. According to the present invention, a luminous efficiency, a color purity and a lifespan of the element can be improved and a driving voltage can be lowered. The organic electric element comprises: an anode; a cathode; and an organic material layer formed between the anode and the cathode.

COMPOUND FOR ORGANIC ELECTRIC ELEMENT AND ORGANIC ELECTRIC DEVICE COMPRISING THE SAME

The present invention relates to a compound for an organic electronic element and an organic electronic element using the same. To the present invention, an organic electronic element having high luminous efficiency, low driving voltage, and high heat resistance can be provided and the color purity and lifetime of the organic electronic element can be improved. (by machine translation)