618442-57-2

Usage

Uses

Used in Organic Synthesis:
9-Phenyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is utilized as a precursor in organic synthesis, particularly for cross-coupling reactions. Its boron-containing groups facilitate the formation of new carbon-carbon or carbon-heteroatom bonds, which are crucial for constructing complex organic molecules.
Used in Organic Electronic Materials Development:
In the field of materials science, 9-Phenyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is used as a building block for the creation of organic electronic materials. Its incorporation in devices such as organic light-emitting diodes (OLEDs) is driven by its potential to enhance the performance and efficiency of these technologies.
Used in Cancer Treatment:
9-Phenyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is also considered for use in boron neutron capture therapy (BNCT), a targeted cancer treatment. The presence of boron in the molecule allows for selective absorption of neutrons, leading to the destruction of cancerous cells while minimizing damage to surrounding healthy tissue.
Used in Pharmaceutical Industry:
9-Phenyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structural features can be leveraged to develop new drugs with specific therapeutic properties.
Used in Chemical Research:
In the academic and research sectors, 9-Phenyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole serves as a subject of study for understanding the reactivity and behavior of boron-containing organic compounds, potentially leading to new insights and applications in chemical synthesis and material development.

Upstream product

• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 57103-20-5 3,6-dibromo-9-phenyl-9H-carbazole 
• 73183-34-3 bis(pinacol)diborane 
• 86-74-8 9H-carbazole 
• 1150-62-5 N-phenylcarbazole 
• 591-50-4 iodobenzene 
• 109-72-8 n-butyllithium 

Downstream Products

• 915224-45-2 C₃₆H₂₉NO₄ 
• 1258780-50-5 9-phenyl-3,6-bis(4-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)-9H-carbazole 
• 1314320-95-0 3,6-di(anthracen-9-yl)-9-phenyl-9H-carbazole 
• 1499166-96-9 9-phenyl-3,6-bis(2-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)-9H-carbazole 
• 1499166-97-0 9-phenyl-3,6-bis(3-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)-9H-carbazole 
• 1141757-83-6 3,6-bis(9'-phenyl-9Η-carbazol-3-yl)-9-phenyl-9H-carbazole 
• 1352413-42-3 C₅₆H₃₇N₅ 
• 1004758-60-4 C₆₈H₄₁N 

Relevant academic research and scientific papers

Synthesis, properties, and electrogenerated chemiluminescence (ECL) of a novel carbazole-based chromophore

A novel molecule containing electron-rich carbazole and electron-deficient pyrimidine moieties exhibits useful and intriguing physical properties, including promising reversible redox behavior that gives rise to electrogenerated chemiluminescence (ECL).

Monomer compounds comprising uracil group, Organic layers comprising the cross-linked of the monomer compounds, and Organic electronic device comprising the organic layers

The present invention provides a pyrimidine-based functional group-containing monomolecular compound represented by chemical formula 1 of Ar-(R_1-R_2-Py)_n as a material for an organic layer of an organic electronic device. The compound can form an organic layer within a short time through photo-curing at room temperature. In chemical formula 1, n is 2-10; Ar is a substituted or non-substituted C_6-C_60 aryl group, or a substituted or non-substituted C_3-C_60 heteroaryl group having an n-valent linking group; each of R_1 and R_2 independently represents a single bond, -O-, a substituted or non-substituted C_6-C_30 arylene group, a substituted or non-substituted C_3-C_30 heteroarylene group, a substituted or non-substituted C_1-C_10 alkylene group, a substituted or non-substituted C_1-C10 alkoxylene group, a substituted or non-substituted amide group, or a substituted or non-substituted amine group; and Py is a monovalent linking group derived from a pyrimidine-based functional group.COPYRIGHT KIPO 2020

CONDENSED CYCLIC COMPOUND, ORGANIC LIGHT-EMITTING DEVICE INCLUDING SAME, AND ELECTRONIC DEVICE INCLUDING ORGANIC LIGHT-EMITTING DEVICE

Provided are a condensed cyclic compound, an organic light-emitting device including the condensed cyclic compound, and an electronic device including the organic light-emitting device. The condensed cyclic compound is represented by Formula 1, wherein R12 is a group represented by Formula 2-1 and R13 is a group represented by Formula 2-2.

N hetero dicarbazyl compound, preparation method of N hetero dicarbazyl compound, intermediate, application and organic electroluminescence device

The invention relates to the field of organic electroluminescence and particularly relates to an N hetero dicarbazyl compound, a preparation method of the N hetero dicarbazyl compound, an intermediate, an application and an organic electroluminescence device. The N hetero dicarbazyl compound is a compound as shown in the formula (1). The provided N hetero dicarbazyl compound can serve as a material for forming the organic electroluminescence device, particularly a material in an electron transmission layer and/or luminescent layer, so that the performances of the organic electroluminescence device are improved, for example, the service life is prolonged, and the efficiency and the brightness are improved.

An electroluminescent compound and an electroluminescent device comprising the same

The present invention relates to an organic light emitting compound employed in an organic electroluminescent device. The organic light emitting compound is represented by chemical formula 1 or chemical formula 2. In addition, the organic electroluminescent device having excellent light emitting properties such as driving voltage, brightness, long lifespan, and the like is implemented when employing the organic light emitting compound as a phosphorescent host compound inside a hole transport functional layer or a light emitting layer.COPYRIGHT KIPO 2016

An electroluminescent compound and an electroluminescent device comprising the same

The present invention relates to an organic light emitting compound applied to an organic light emitting device. The organic light emitting compound: is represented by chemical formula 1; includes one or more substituted bodies represented by structural formula 1 or structural formula 2; and is capable of realizing an organic light emitting device having excellent luminous properties such as driving voltage, luminance, a long life and the like in the case of being applied as a phosphorescent host compound in a hole transporting functional layer or an emissive layer.COPYRIGHT KIPO 2016

Highly efficient deep-blue emitting organic light emitting diode based on the multifunctional fluorescent molecule comprising covalently bonded carbazole and anthracene moieties

High performance deep-blue organic light-emitting diodes (OLEDs) have been investigated using new multifunctional blue emitting materials 3-(anthracen-9-yl)-9-ethyl-9H-carbazole (AC), 3,6-di(anthracen-9-yl)-9-ethyl-9H- carbazole (DAC), 3-(anthracen-9-yl-)-9-phenyl-9H-carbazole (P-AC), and 3,6-di(anthracen-9-yl)-9-phenyl-9H-carbazole (P-DAC) which comprise covalently bonded carbazole and anthracene moieties. We also have investigated the thermal, electrochemical, and morphological stability to find suitable molecular structure, consisting of carbazole and anthracene moieties. The non-doping deep-blue OLEDs using P-DAC, which showed the highest thermal, electrochemical, and morphological stability, proved the highest luminance efficiency and external quantum efficiency of 3.14 cd A-1 and 2.75%, with the Commission Internationale de l'Eclairage (CIE) chromaticity coordinates (0.162, 0.136) at 100 mA cm-2. Moreover, the doping devices using P-DAC as the host material showed blue emission, and the high luminance efficiencies and external quantum efficiencies of as high as 7.70 cd A-1 and 4.86% with CIE chromaticity coordinates (0.156, 0.136) and (0.156, 0.217) at 100 mA cm-2. Both the non-doping and doping devices using P-DAC uniquely exhibited high operational stability with virtually negligible efficiency roll-off over the broad current density range.

Electron transport agents for organic electronic devices

Compounds and compositions are provided that can be used as electron transport agents in organic electronic devices such as organic electroluminescent devices. The compounds are non-polymeric and have an aromatic core conjugated to end capping groups. The aromatic core contains a phenylene group arylene or naphthalene group arylene having a pendant heteroaryl group that includes a —C═N— unit.

Electroactive polymers

Electroactive polymeric arylenes and intermediates useful for making such polymers are disclosed. The present invention also provides electroactive compositions comprising the electroactive polymeric arylenes, organic electronic devices which comprise these polymers and compositions, and methods of fabricating these devices.

Syntheses and structures of novel heteroarene-fused coplanar π-conjugated chromophores

(Chemical Equation Presented) We have synthesized a series of novel coplanar chromophores in which heteroarenes, namely, thiophene, benzothiophene, and carbazole, were fused to neighboring phenylene ring(s) through intramolecular annulation via sp3/