[1,1'-Binaphthalen]-4-ylboronic acid
98%
Reagent
Code: #90323
CAS Number
363607-69-6
science Other reagents with same CAS 363607-69-6
blur_circular Chemical Specifications
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Molecular Information
Weight
298.14 g/mol
Formula
C₂₀H₁₅BO₂
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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.
format_list_bulleted Product Specification
| 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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