[3-(9-phenylcarbazol-3-yl)phenyl]boronic acid

98%

Reagent Code: #227815
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CAS Number 854952-60-6

science Other reagents with same CAS 854952-60-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 363.2 g/mol
Formula C₂₄H₁₈BNO₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct complex aromatic frameworks. Its boronic acid functionality enables efficient carbon-carbon bond formation, making it valuable in the development of organic electronic materials, such as OLEDs and hole-transport materials. The carbazole moiety contributes to high thermal stability and good hole-transport properties, enhancing performance in optoelectronic devices. Also employed in the synthesis of conjugated polymers and small-molecule semiconductors for use in organic photovoltaics and field-effect transistors.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,300.00
1g
10-20 days ฿3,660.00
5g
10-20 days ฿11,720.00
[3-(9-phenylcarbazol-3-yl)phenyl]boronic acid
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Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct complex aromatic frameworks. Its boronic acid functionality enables efficient carbon-carbon bond formation, making it valuable in the development of organic electronic materials, such as OLEDs and hole-transport materials. The carbazole moiety contributes to high thermal stability and good hole-transport properties, enhancing performance in optoelectronic devices. Also employed in the syn

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct complex aromatic frameworks. Its boronic acid functionality enables efficient carbon-carbon bond formation, making it valuable in the development of organic electronic materials, such as OLEDs and hole-transport materials. The carbazole moiety contributes to high thermal stability and good hole-transport properties, enhancing performance in optoelectronic devices. Also employed in the synthesis of conjugated polymers and small-molecule semiconductors for use in organic photovoltaics and field-effect transistors.

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