3’-(9-Carbazolyl)Biphenyl-3-Boronic Acid

≥98%

Reagent Code: #91057
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CAS Number 854952-42-4

science Other reagents with same CAS 854952-42-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 363.21 g/mol
Formula C₂₄H₁₈BNO₂
badge Registry Numbers
MDL Number MFCD26406216
thermostat Physical Properties
Boiling Point 579.6±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.18±0.1 g/cm3(Predicted)
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of organic electronic materials, including OLEDs (Organic Light-Emitting Diodes) and other optoelectronic devices. Its carbazole moiety enhances charge transport properties, making it valuable in the development of high-performance light-emitting materials. Additionally, it is employed in the synthesis of complex organic molecules for pharmaceutical research, where its boronic acid group facilitates the formation of carbon-carbon bonds. Its unique structure also makes it suitable for use in the design of advanced polymers and coatings with specific optical or electronic characteristics.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,071.00
inventory 5g
10-20 days ฿3,555.00
inventory 25g
10-20 days ฿17,082.00

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3’-(9-Carbazolyl)Biphenyl-3-Boronic Acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of organic electronic materials, including OLEDs (Organic Light-Emitting Diodes) and other optoelectronic devices. Its carbazole moiety enhances charge transport properties, making it valuable in the development of high-performance light-emitting materials. Additionally, it is employed in the synthesis of complex organic molecules for pharmaceutical research, where its boronic acid group facilitates the formation of carbon-carbon bonds. Its unique structure also makes it suitable for use in the design of advanced polymers and coatings with specific optical or electronic characteristics.
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