(S)-3,3’-Bis(triphenylsilyl)-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
≥98%,≥99%e.e.
- Product Code: 65626
| Molecular Weight: | 811.2 g./mol | Molecular Formula: | C₅₆H₅₀O₂Si₂ |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring a binaphthol core with triphenylsilyl groups, enhances stereoselectivity in various organic reactions, such as hydrogenation, allylic alkylation, and Diels-Alder reactions. It is also employed in the synthesis of enantiomerically pure compounds, which are crucial in pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a chiral auxiliary in the preparation of complex molecules, enabling precise control over stereochemistry. Its stability and steric properties make it a valuable tool in advanced synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿21,861.00 |
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(S)-3,3’-Bis(triphenylsilyl)-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring a binaphthol core with triphenylsilyl groups, enhances stereoselectivity in various organic reactions, such as hydrogenation, allylic alkylation, and Diels-Alder reactions. It is also employed in the synthesis of enantiomerically pure compounds, which are crucial in pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a chiral auxiliary in the preparation of complex molecules, enabling precise control over stereochemistry. Its stability and steric properties make it a valuable tool in advanced synthetic methodologies.
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