243-28-7

Usage

Synthesis Reference(s)

Tetrahedron Letters, 24, p. 5435, 1983 DOI: 10.1016/S0040-4039(00)94105-4

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

Upstream product

• 26211-73-4 (2-methyl-1H-indol-3-yl)phenylmethanone 
• 854161-68-5 1-(naphthalen-2-yl)-1H-benzo[d][1,2,3]triazole 
• 135-88-6 N-Phenyl-2-naphthylamine 
• 22013-66-7 5-(2-Naphthoyl)-5H-benzocarbazole 
• 21064-53-9 1-benzo[b]carbazol-5-yl-ethanone 
• 89241-40-7 5-(phenylsulfonyl)-6,11-epoxy-6,11-dihydro-5H-benzocarbazole 
• 580-13-2 2-bromonaphthalene 
• 55583-72-7 N-[2]naphthyl-o-phenylenediamine 
• 854161-86-7 3-[2]naphthyl-3H-benzotriazole-4-carboxylic acid 
• 76783-56-7 N-(2-chlorophenyl)naphthalen-2-amine 
• 1609211-24-6 C₂₂H₁₆N₂O 
• 615-36-1 2-bromoaniline 
• 32316-92-0 naphthalene-2-boronic acid 
• 71221-26-6 2-(2-naphthyl)aniline 

Downstream Products

• 88-99-3 benzene-1,2-dicarboxylic acid 

Relevant academic research and scientific papers

Benzocarbazole Synthesis via Visible-Light-Accelerated Rh(III)-Catalyzed C-H Annulation of Aromatic Amines with Bicyclic Alkenes

A visible-light-accelerated Rh(III)-catalyzed C-H annulation of aromatic amines with bicyclic alkenes for the synthesis of benzocarbazole derivatives was developed. In this approach, with the cooperation of rhodium catalysis and visible-light irradiation, various aromatic amines reacted with oxabicyclic alkenes and azabicyclic alkenes smoothly at room temperature, delivering the corresponding bridged oxa or aza tetrahydro benzocarbazoles in good to excellent yields. Moreover, a series of benzo[b]carbazoles were synthesized conveniently through further aromatization in one pot. The potential of this method was demonstrated via directing-group removal, derivatization, a scale-up reaction, and fluorescence investigations.

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The present invention provides a novel heterocyclic compound and an organic light emitting device using the same.

Novel hetero-cyclic compound and organic light emitting device comprising the same

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The present invention provides a novel compound and an organic light emitting device using the same. The present invention provides a compound represented by chemical formula 1. The compound represented by chemical formula 1 can be used as a material for an organic layer of the organic light emitting device, and can improve efficiency, low driving voltage, and/or lifespan characteristics in the organic light emitting device.

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The present invention provides a novel compound and an organic light emitting device using the same. The present invention provides a compound represented by chemical formula 1. The compound represented by chemical formula 1 can be used as a material for an organic material layer of the organic light emitting device, thereby improving the efficiency, low driving voltage and/or lifespan characteristics of the organic light emitting device.

Novel compound and organic light emitting device comprising the same

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