(2S,3S,4aR,8aR)-2,3-bis(2-(diphenylphosphaneyl)phenyl)-1,4-dimethyldecahydroquinoxaline
98%,99%ee
- Product Code: 121147
CAS:
1562581-18-3
| Molecular Weight: | 688.82 g./mol | Molecular Formula: | C₄₆H₄₆N₂P₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30833872 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure, featuring diphenylphosphine groups and a rigid decahydroquinoxaline backbone, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation reactions, where it helps produce chiral molecules with high enantiomeric purity, crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, its stability and selectivity make it suitable for use in cross-coupling reactions, enabling the formation of complex organic compounds with precise stereochemical control.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿13,500.00 |
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(2S,3S,4aR,8aR)-2,3-bis(2-(diphenylphosphaneyl)phenyl)-1,4-dimethyldecahydroquinoxaline
This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure, featuring diphenylphosphine groups and a rigid decahydroquinoxaline backbone, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation reactions, where it helps produce chiral molecules with high enantiomeric purity, crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, its stability and selectivity make it suitable for use in cross-coupling reactions, enabling the formation of complex organic compounds with precise stereochemical control.
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