[S(R)]-N-[(1R)-1-[5-(Diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl]-2,2-dimethylpropyl]-2-methyl-2-propanesulfinamide
95%
- Product Code: 236680
CAS:
2162939-92-4
| Molecular Weight: | 583.76 g./mol | Molecular Formula: | C₃₆H₄₂NO₂PS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32697193 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, argon |
Product Description:
Widely used as a chiral ligand precursor in asymmetric catalysis, this compound plays a key role in the synthesis of enantiomerically enriched molecules. It is particularly effective in palladium-catalyzed asymmetric allylic alkylation reactions, where it helps achieve high enantioselectivity. The rigid xanthene backbone and tunable phosphine group enhance metal coordination and stereocontrol. Due to its steric bulk and well-defined chiral environment, it enables efficient asymmetric induction in the formation of carbon–carbon and carbon–heteroatom bonds. It is commonly employed in pharmaceutical and fine chemical synthesis where precise stereochemistry is critical.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 5mg | 10-20 days | $72.67 |
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| 25mg | 10-20 days | $254.09 |
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[S(R)]-N-[(1R)-1-[5-(Diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl]-2,2-dimethylpropyl]-2-methyl-2-propanesulfinamide
Widely used as a chiral ligand precursor in asymmetric catalysis, this compound plays a key role in the synthesis of enantiomerically enriched molecules. It is particularly effective in palladium-catalyzed asymmetric allylic alkylation reactions, where it helps achieve high enantioselectivity. The rigid xanthene backbone and tunable phosphine group enhance metal coordination and stereocontrol. Due to its steric bulk and well-defined chiral environment, it enables efficient asymmetric induction in the formation of carbon–carbon and carbon–heteroatom bonds. It is commonly employed in pharmaceutical and fine chemical synthesis where precise stereochemistry is critical.
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