(S)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-diphenyl-[1,1'-binaphthalene]-2,2'-diol
≥98%,99%e.e.
- Product Code: 125058
CAS:
575451-08-0
| Molecular Weight: | 446.6 g./mol | Molecular Formula: | C₃₂H₃₀O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 186-190°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce optically active compounds with high enantiomeric excess. Additionally, it serves as a key component in the preparation of chiral catalysts for organic transformations, including C-C bond formation reactions. Its rigid binaphthyl structure and chiral centers make it effective in inducing stereochemical control, which is essential in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft31,244.91 |
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| 0.250 | 10-20 days | Ft55,809.88 |
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(S)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-diphenyl-[1,1'-binaphthalene]-2,2'-diol
This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce optically active compounds with high enantiomeric excess. Additionally, it serves as a key component in the preparation of chiral catalysts for organic transformations, including C-C bond formation reactions. Its rigid binaphthyl structure and chiral centers make it effective in inducing stereochemical control, which is essential in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.
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