(S)-N-((S)-(5-(Diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl)(2-isopropylphenyl)methyl)-2-methylpropane-2-sulfinamide
98%
- Product Code: 237780
CAS:
2374225-96-2
| Molecular Weight: | 645.83 g./mol | Molecular Formula: | C₄₁H₄₄NO₂PS |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations, particularly in rhodium- and ruthenium-catalyzed asymmetric hydrogenation reactions. It is highly effective in the synthesis of chiral amines, alcohols, and other stereochemically complex molecules important in pharmaceutical manufacturing. Due to its well-defined chiral environment and strong coordination to transition metals, it enables high enantioselectivity and catalytic efficiency. Its application is especially valuable in the development of active pharmaceutical ingredients (APIs) where control of stereochemistry is critical for biological activity and regulatory approval.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25mg | 10-20 days | $285.64 |
+
-
|
| 50mg | 10-20 days | $510.86 |
+
-
|
| 100mg | 10-20 days | $843.13 |
+
-
|
(S)-N-((S)-(5-(Diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl)(2-isopropylphenyl)methyl)-2-methylpropane-2-sulfinamide
Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations, particularly in rhodium- and ruthenium-catalyzed asymmetric hydrogenation reactions. It is highly effective in the synthesis of chiral amines, alcohols, and other stereochemically complex molecules important in pharmaceutical manufacturing. Due to its well-defined chiral environment and strong coordination to transition metals, it enables high enantioselectivity and catalytic efficiency. Its application is especially valuable in the development of active pharmaceutical ingredients (APIs) where control of stereochemistry is critical for biological activity and regulatory approval.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Purchase History for
Loading purchase history...
Cart
No products
Subtotal:
$0.00
$0.00
Total :