[2,2'-Binaphthalene]-6,6'-dicarboxylic acid

≥95%

Reagent Code: #86928
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CAS Number 932033-58-4

science Other reagents with same CAS 932033-58-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 342.34 g/mol
Formula C₂₂H₁₄O₄
badge Registry Numbers
MDL Number MFCD26142857
inventory_2 Storage & Handling
Storage Room temperature, away from light, dry, sealed

description Product Description

This chemical is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a key building block for the preparation of chiral ligands, which are essential in enantioselective reactions. These ligands are often employed in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions, enabling the production of optically active compounds. Additionally, it is used in the development of chiral stationary phases for high-performance liquid chromatography (HPLC), aiding in the separation of enantiomers in pharmaceutical and chemical industries. Its rigid binaphthyl structure also makes it a valuable component in the design of supramolecular assemblies and functional materials, including sensors and molecular devices.

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Test Parameter Specification
Appearance Off-White to Light Yellow Solid
Purity (%) 95-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿12,564.00
inventory 250mg
10-20 days ฿4,986.00
inventory 100mg
10-20 days ฿3,384.00

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[2,2'-Binaphthalene]-6,6'-dicarboxylic acid
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This chemical is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a key building block for the preparation of chiral ligands, which are essential in enantioselective reactions. These ligands are often employed in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions, enabling the production of optically active compounds. Additionally, it is used in the development of chiral stationary phases for high-performan

This chemical is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a key building block for the preparation of chiral ligands, which are essential in enantioselective reactions. These ligands are often employed in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions, enabling the production of optically active compounds. Additionally, it is used in the development of chiral stationary phases for high-performance liquid chromatography (HPLC), aiding in the separation of enantiomers in pharmaceutical and chemical industries. Its rigid binaphthyl structure also makes it a valuable component in the design of supramolecular assemblies and functional materials, including sensors and molecular devices.

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