[2,2'-Binaphthalene]-6,6'-dicarboxylic acid
≥95%
- Product Code: 86928
CAS:
932033-58-4
| Molecular Weight: | 342.34 g./mol | Molecular Formula: | C₂₂H₁₄O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26142857 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, away from light, dry, sealed |
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,384.00 |
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| 0.250 | 10-20 days | ฿4,986.00 |
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| 1.000 | 10-20 days | ฿12,564.00 |
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[2,2'-Binaphthalene]-6,6'-dicarboxylic acid
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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