1-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole

98%

Reagent Code: #243320
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CAS Number 1219637-88-3

science Other reagents with same CAS 1219637-88-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.17 g/mol
Formula C₁₈H₂₀BNO₂
badge Registry Numbers
MDL Number MFCD29112189
thermostat Physical Properties
Boiling Point 474.3±18.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.16±0.1 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Widely used in organic synthesis, particularly in palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key building block for constructing conjugated organic materials, especially in the development of organic semiconductors and optoelectronic devices. Commonly employed in the synthesis of organic light-emitting diodes (OLEDs), where carbazole derivatives contribute to hole-transport properties and enhance device efficiency and stability. Also utilized in the preparation of organic photovoltaics (OPVs) and perovskite solar cells due to its ability to form stable, conjugated frameworks with tunable electronic properties. Its boron-containing group enables reliable and selective coupling, making it valuable in the fabrication of complex aromatic systems for advanced materials research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,390.00
inventory 5g
10-20 days ฿9,030.00
inventory 1g
10-20 days ฿2,560.00

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1-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
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Widely used in organic synthesis, particularly in palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key building block for constructing conjugated organic materials, especially in the development of organic semiconductors and optoelectronic devices. Commonly employed in the synthesis of organic light-emitting diodes (OLEDs), where carbazole derivatives contribute to hole-transport properties and enhance device efficiency and stability. Also utilized in the preparation of organic photovoltaics (OPVs) and perovskite solar cells due to its ability to form stable, conjugated frameworks with tunable electronic properties. Its boron-containing group enables reliable and selective coupling, making it valuable in the fabrication of complex aromatic systems for advanced materials research.
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