9-([1, 1'-Biphenyl]-4-yl)-2-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)-9H-carbazole

97%

Reagent Code: #151992
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CAS Number 1427213-44-2

science Other reagents with same CAS 1427213-44-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 445.36 g/mol
Formula C₃₀H₂₈BNO₂
badge Registry Numbers
MDL Number MFCD32670107
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Widely used in organic electronics, this compound serves as a key intermediate in the synthesis of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its structure supports efficient charge transport and enhances device performance due to strong conjugation and thermal stability. The boronic ester group enables cross-coupling reactions, especially Suzuki-Miyaura coupling, allowing for the construction of complex conjugated systems used in emissive layers or host materials in OLEDs. It is also employed in the development of hole-transport materials and blue emitters, where its biphenyl and carbazole moieties contribute to high triplet energy levels and good morphological stability. Its compatibility with solution-processing techniques makes it suitable for low-cost, large-area optoelectronic devices.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,520.00
inventory 5g
10-20 days ฿12,340.00
inventory 10g
10-20 days ฿22,400.00

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9-([1, 1'-Biphenyl]-4-yl)-2-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)-9H-carbazole
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Widely used in organic electronics, this compound serves as a key intermediate in the synthesis of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its structure supports efficient charge transport and enhances device performance due to strong conjugation and thermal stability. The boronic ester group enables cross-coupling reactions, especially Suzuki-Miyaura coupling, allowing for the construction of complex conjugated systems used in emissive layers or host materials in OLEDs. I

Widely used in organic electronics, this compound serves as a key intermediate in the synthesis of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its structure supports efficient charge transport and enhances device performance due to strong conjugation and thermal stability. The boronic ester group enables cross-coupling reactions, especially Suzuki-Miyaura coupling, allowing for the construction of complex conjugated systems used in emissive layers or host materials in OLEDs. It is also employed in the development of hole-transport materials and blue emitters, where its biphenyl and carbazole moieties contribute to high triplet energy levels and good morphological stability. Its compatibility with solution-processing techniques makes it suitable for low-cost, large-area optoelectronic devices.

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