(R)-2,2'-Dimethoxy-1,1'-binaphthalene
≥98%,99%e.e.
- Product Code: 70294
CAS:
35294-28-1
| Molecular Weight: | 314.4 g./mol | Molecular Formula: | C₂₂H₁₈O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 227-231°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
(R)-2,2'-Dimethoxy-1,1'-binaphthalene is widely used as a chiral ligand in asymmetric synthesis. It plays a crucial role in catalytic reactions, particularly in the formation of chiral centers in organic molecules. This compound is often employed in transition metal-catalyzed reactions, such as asymmetric hydrogenation and carbon-carbon bond-forming reactions, to produce enantiomerically pure compounds. Its application is significant in the pharmaceutical industry, where it aids in the synthesis of chiral drugs, ensuring high enantioselectivity and efficiency. Additionally, it is utilized in the development of advanced materials and in academic research to study chiral induction and catalysis mechanisms.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-White Solid, Powder, or Crystals |
| PURITY | 98-100 |
| MELTING POINT | 230-234 |
| Infrared spectrum | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
| Specific rotation 20DC1.2 THF | 70 |
| e.e | 99-100 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $193.82 |
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| 25.000 | 10-20 days | $740.47 |
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(R)-2,2'-Dimethoxy-1,1'-binaphthalene
(R)-2,2'-Dimethoxy-1,1'-binaphthalene is widely used as a chiral ligand in asymmetric synthesis. It plays a crucial role in catalytic reactions, particularly in the formation of chiral centers in organic molecules. This compound is often employed in transition metal-catalyzed reactions, such as asymmetric hydrogenation and carbon-carbon bond-forming reactions, to produce enantiomerically pure compounds. Its application is significant in the pharmaceutical industry, where it aids in the synthesis of chiral drugs, ensuring high enantioselectivity and efficiency. Additionally, it is utilized in the development of advanced materials and in academic research to study chiral induction and catalysis mechanisms.
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