(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-2,2'-diisopropyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole
≥97% ,≥99% ee
- Product Code: 96545
CAS:
2207601-12-3
| Molecular Weight: | 470.56 g./mol | Molecular Formula: | C₂₈H₄₀O₂P₂ |
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| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis as a chiral ligand or catalyst. Its unique stereochemistry makes it highly effective in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is often employed in transition metal-catalyzed processes, such as hydrogenation, hydroformylation, and cross-coupling reactions, where high enantiomeric purity of the product is desired. Additionally, its robust structure and steric properties enhance its stability and performance in demanding reaction conditions, making it a valuable tool in the synthesis of pharmaceuticals, fine chemicals, and advanced materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.025 | 10-20 days | €165.97 |
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| 0.100 | 10-20 days | €474.64 |
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(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-2,2'-diisopropyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole
This compound is primarily utilized in the field of asymmetric synthesis as a chiral ligand or catalyst. Its unique stereochemistry makes it highly effective in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is often employed in transition metal-catalyzed processes, such as hydrogenation, hydroformylation, and cross-coupling reactions, where high enantiomeric purity of the product is desired. Additionally, its robust structure and steric properties enhance its stability and performance in demanding reaction conditions, making it a valuable tool in the synthesis of pharmaceuticals, fine chemicals, and advanced materials.
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