[1,1'-Binaphthalen]-4-ylboronic acid

98%

Reagent Code: #90323
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CAS Number 363607-69-6

science Other reagents with same CAS 363607-69-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.14 g/mol
Formula C₂₀H₁₅BO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis as a building block for creating complex molecules. It is often employed in Suzuki-Miyaura cross-coupling reactions, which are widely used to form carbon-carbon bonds. The boronic acid group in this compound makes it a valuable reagent for coupling with aryl halides, enabling the synthesis of biaryl structures. These structures are significant in the development of pharmaceuticals, agrochemicals, and organic materials. Additionally, its binaphthyl backbone can impart chirality, making it useful in asymmetric synthesis and the production of chiral catalysts or ligands for enantioselective reactions. Its application extends to materials science, where it can be used to design advanced polymers or organic electronic materials.

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Test Parameter Specification
Appearance White to gray to brown powder to crystal
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,700.00

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[1,1'-Binaphthalen]-4-ylboronic acid
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This compound is primarily utilized in organic synthesis as a building block for creating complex molecules. It is often employed in Suzuki-Miyaura cross-coupling reactions, which are widely used to form carbon-carbon bonds. The boronic acid group in this compound makes it a valuable reagent for coupling with aryl halides, enabling the synthesis of biaryl structures. These structures are significant in the development of pharmaceuticals, agrochemicals, and organic materials. Additionally, its binaphthyl backbone can impart chirality, making it useful in asymmetric synthesis and the production of chiral catalysts or ligands for enantioselective reactions. Its application extends to materials science, where it can be used to design advanced polymers or organic electronic materials.
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