(R)-3,3'-Bis(triphenylsilyl)-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
≥95%,99%e.e.
- Product Code: 70363
CAS:
1041186-22-4
| Molecular Weight: | 811.2 g./mol | Molecular Formula: | C₅₆H₅₀O₂Si₂ |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its structure, featuring chiral centers and bulky triphenylsilyl groups, makes it an effective ligand for transition metal catalysts. It is often employed in the development of chiral catalysts for organic transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Additionally, it finds application in the synthesis of complex natural products and pharmaceuticals, where high enantiomeric purity is crucial. Its unique steric and electronic properties enhance the selectivity and efficiency of catalytic processes, making it valuable in advanced synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿22,580.00 |
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(R)-3,3'-Bis(triphenylsilyl)-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its structure, featuring chiral centers and bulky triphenylsilyl groups, makes it an effective ligand for transition metal catalysts. It is often employed in the development of chiral catalysts for organic transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Additionally, it finds application in the synthesis of complex natural products and pharmaceuticals, where high enantiomeric purity is crucial. Its unique steric and electronic properties enhance the selectivity and efficiency of catalytic processes, making it valuable in advanced synthetic chemistry.
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