(R)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-bis(4-nitrophenyl)-[1,1'-binaphthalene]-2,2'-diol
≥98%,99%e.e.
- Product Code: 70344
CAS:
791616-67-6
| Molecular Weight: | 536.6 g./mol | Molecular Formula: | C₃₂H₂₈N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 727.9±60.0 °C | |
| Density: | 1.343±0.06 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in enantioselective reactions, particularly in the formation of chiral molecules, which are crucial in the pharmaceutical industry for producing drugs with high stereochemical purity. Its structure allows it to effectively induce asymmetry in reactions like hydrogenation, oxidation, and carbon-carbon bond formation. Additionally, it is employed in the development of advanced materials and sensors, where its chiral properties enhance selectivity and performance.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,790.00 |
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| 0.250 | 10-20 days | ฿8,950.00 |
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(R)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-bis(4-nitrophenyl)-[1,1'-binaphthalene]-2,2'-diol
This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in enantioselective reactions, particularly in the formation of chiral molecules, which are crucial in the pharmaceutical industry for producing drugs with high stereochemical purity. Its structure allows it to effectively induce asymmetry in reactions like hydrogenation, oxidation, and carbon-carbon bond formation. Additionally, it is employed in the development of advanced materials and sensors, where its chiral properties enhance selectivity and performance.
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