(9-([1,1'-Biphenyl]-3-yl)-9H-carbazol-3-yl)boronic acid

95%

Reagent Code: #154631
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CAS Number 1416814-68-0

science Other reagents with same CAS 1416814-68-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 363.22 g/mol
Formula C₂₄H₁₈BNO₂
badge Registry Numbers
MDL Number MFCD27979929
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for constructing biaryl 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 semiconducting polymers. Commonly employed in the synthesis of conjugated molecules for optoelectronic devices due to the combined electron-transport properties of the carbazole and biphenyl moieties. Also utilized in pharmaceutical research for building complex aromatic structures with potential bioactivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,330.00
inventory 1g
10-20 days ฿38,640.00

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(9-([1,1'-Biphenyl]-3-yl)-9H-carbazol-3-yl)boronic acid
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Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for constructing biaryl 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 semiconducting polymers. Commonly employed in the synthesis of conjugated molecules for optoelectronic devices due to the combined electron-transport properties of the carbazole and biphenyl moieties.

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for constructing biaryl 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 semiconducting polymers. Commonly employed in the synthesis of conjugated molecules for optoelectronic devices due to the combined electron-transport properties of the carbazole and biphenyl moieties. Also utilized in pharmaceutical research for building complex aromatic structures with potential bioactivity.

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