2-(9H-Carbazol-9-yl)phenylboronic Acid

97%, containing different amounts of acid anhydride

Reagent Code: #89645
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CAS Number 1189047-28-6

science Other reagents with same CAS 1189047-28-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.13 g/mol
Formula C₁₈H₁₄BNO₂
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Storage room temperature

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the development of organic light-emitting diodes (OLEDs) and other optoelectronic materials. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the creation of complex organic molecules with high precision. Additionally, it is employed in the preparation of carbazole-based polymers, which are valued for their thermal stability and hole-transporting properties in electronic devices. Researchers also utilize it in the study of luminescent materials for potential applications in sensors and bioimaging.

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Test Parameter Specification
Appearance White to Off-White Powder or Crystals
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 200mg
10-20 days ฿4,581.00

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2-(9H-Carbazol-9-yl)phenylboronic Acid
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Used primarily in organic synthesis, this compound serves as a key intermediate in the development of organic light-emitting diodes (OLEDs) and other optoelectronic materials. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the creation of complex organic molecules with high precision. Additionally, it is employed in the preparation of carbazole-based polymers, which are valued for their thermal stability and hole-transporting properties in electr

Used primarily in organic synthesis, this compound serves as a key intermediate in the development of organic light-emitting diodes (OLEDs) and other optoelectronic materials. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the creation of complex organic molecules with high precision. Additionally, it is employed in the preparation of carbazole-based polymers, which are valued for their thermal stability and hole-transporting properties in electronic devices. Researchers also utilize it in the study of luminescent materials for potential applications in sensors and bioimaging.

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