(R)-3,3'-Bis(4-methoxyphenyl)-[1,1'-binaphthalene]-2,2'-diol
≥98%,99%e.e.
- Product Code: 70334
CAS:
756491-51-7
| Molecular Weight: | 498.6 g./mol | Molecular Formula: | C₃₄H₂₆O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 109-111°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where the production of a specific enantiomer is crucial for biological activity or desired properties. Additionally, it finds application in the development of chiral catalysts for organic transformations, such as hydrogenation, oxidation, and carbon-carbon bond formation. Its unique structure and chirality make it valuable in research and industrial processes aimed at achieving precise stereochemical control.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White to off-white solid |
| Purity | 97.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿5,200.00 |
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| 100mg | 10-20 days | ฿3,090.00 |
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| 1g | 10-20 days | ฿11,200.00 |
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(R)-3,3'-Bis(4-methoxyphenyl)-[1,1'-binaphthalene]-2,2'-diol
This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where the production of a specific enantiomer is crucial for biological activity or desired properties. Additionally, it finds application in the development of chiral catalysts for organic transformations, such as hydrogenation, oxidation, and carbon-carbon bond formation. Its unique structure and chirality make it valuable in research and industrial processes aimed at achieving precise stereochemical control.
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| Stable in pH range | - |
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