(R)-3,3'-Bis(triphenylsilyl)-[1,1'-binaphthalene]-2,2'-diol
98%
- Product Code: 230617
CAS:
111822-69-6
| Molecular Weight: | 803.1 g./mol | Molecular Formula: | C₅₆H₄₂O₂Si₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09265078 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its sterically bulky silyl groups enhance stereoselectivity by creating a well-defined chiral environment around the metal center when coordinated. Commonly employed in asymmetric allylic alkylation, Diels-Alder reactions, and other carbon–carbon bond-forming reactions where high enantiomeric excess is required. The compound’s rigid binaphthyl backbone and tunable substituents make it effective in promoting asymmetric induction in transition metal-catalyzed processes. Also utilized in the synthesis of chiral pharmaceuticals and fine chemicals where precise stereochemical control is critical.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | ฿1,170.00 |
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| 100mg | 10-20 days | ฿2,100.00 |
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| 250mg | 10-20 days | ฿4,280.00 |
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| 1g | 10-20 days | ฿14,850.00 |
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(R)-3,3'-Bis(triphenylsilyl)-[1,1'-binaphthalene]-2,2'-diol
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its sterically bulky silyl groups enhance stereoselectivity by creating a well-defined chiral environment around the metal center when coordinated. Commonly employed in asymmetric allylic alkylation, Diels-Alder reactions, and other carbon–carbon bond-forming reactions where high enantiomeric excess is required. The compound’s rigid binaphthyl backbone and tunable substituents make it effective in promoting asymmetric induction in transition metal-catalyzed processes. Also utilized in the synthesis of chiral pharmaceuticals and fine chemicals where precise stereochemical control is critical.
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