(R)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol
≥98%,99%e.e.
- Product Code: 70359
CAS:
65355-08-0
| Molecular Weight: | 452.2 g./mol | Molecular Formula: | C₂₀H₂₀Br₂O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 146-149°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in asymmetric synthesis, serving as a chiral ligand or catalyst in various organic reactions. It is particularly effective in enantioselective transformations, such as hydrogenation, oxidation, and carbon-carbon bond-forming reactions. Its rigid binaphthyl structure and bromine substituents enhance its ability to induce high enantioselectivity, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it is employed in the development of chiral materials and sensors, where precise stereochemical control is essential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿558.00 |
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| 0.200 | 10-20 days | ฿1,062.00 |
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| 1.000 | 10-20 days | ฿3,024.00 |
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| 5.000 | 10-20 days | ฿13,212.00 |
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(R)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol
This chemical is primarily utilized in asymmetric synthesis, serving as a chiral ligand or catalyst in various organic reactions. It is particularly effective in enantioselective transformations, such as hydrogenation, oxidation, and carbon-carbon bond-forming reactions. Its rigid binaphthyl structure and bromine substituents enhance its ability to induce high enantioselectivity, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it is employed in the development of chiral materials and sensors, where precise stereochemical control is essential.
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