(R)-N-((R)-(2-(Di-tert-butylphosphino)phenyl)(phenyl)methyl)-N,2-dimethylpropane-2-sulfinamide
95%
- Product Code: 231402
CAS:
2757083-12-6
| Molecular Weight: | 445.64 g./mol | Molecular Formula: | C₂₆H₄₀NOPS |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, light-proof, inert gas |
Product Description:
Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations, particularly in transition-metal-catalyzed reactions. It is highly effective in palladium-catalyzed asymmetric allylic alkylation and other cross-coupling reactions where control of stereochemistry is critical. The bulky tert-butyl groups and the rigid backbone enhance stereoselectivity by creating a well-defined chiral environment around the metal center. Its sulfinamide moiety allows for easy handling and purification, making it a practical choice in synthetic organic chemistry. It is often employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric excess is required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿7,130.00 |
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| 0.100 | 10-20 days | ฿10,650.00 |
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| 0.250 | 10-20 days | ฿23,120.00 |
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(R)-N-((R)-(2-(Di-tert-butylphosphino)phenyl)(phenyl)methyl)-N,2-dimethylpropane-2-sulfinamide
Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations, particularly in transition-metal-catalyzed reactions. It is highly effective in palladium-catalyzed asymmetric allylic alkylation and other cross-coupling reactions where control of stereochemistry is critical. The bulky tert-butyl groups and the rigid backbone enhance stereoselectivity by creating a well-defined chiral environment around the metal center. Its sulfinamide moiety allows for easy handling and purification, making it a practical choice in synthetic organic chemistry. It is often employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric excess is required.
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