N-[(1S)-2-(Diphenylphosphino)-1-(2-(diphenylphosphino)phenyl)ethyl]-3,5-bis(trifluoromethyl)-benzamide
95%
- Product Code: 68807
CAS:
2249744-81-6
| Molecular Weight: | 729.6 g./mol | Molecular Formula: | C₄₁H₃₁F₆NOP₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in catalysis, particularly in asymmetric synthesis, where it acts as a chiral ligand. Its structure, featuring diphenylphosphino groups and trifluoromethyl substituents, makes it highly effective in facilitating enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transition metal-catalyzed processes. The trifluoromethyl groups enhance its stability and reactivity, making it suitable for use in demanding chemical environments. It is often employed in the pharmaceutical industry for the synthesis of chiral intermediates, which are crucial for producing enantiomerically pure drugs. Additionally, its application extends to materials science, where it aids in the development of advanced polymers and catalysts with specific stereochemical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿12,969.00 |
+
-
|
| 0.500 | 10-20 days | ฿45,387.00 |
+
-
|
N-[(1S)-2-(Diphenylphosphino)-1-(2-(diphenylphosphino)phenyl)ethyl]-3,5-bis(trifluoromethyl)-benzamide
This chemical is primarily used in catalysis, particularly in asymmetric synthesis, where it acts as a chiral ligand. Its structure, featuring diphenylphosphino groups and trifluoromethyl substituents, makes it highly effective in facilitating enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transition metal-catalyzed processes. The trifluoromethyl groups enhance its stability and reactivity, making it suitable for use in demanding chemical environments. It is often employed in the pharmaceutical industry for the synthesis of chiral intermediates, which are crucial for producing enantiomerically pure drugs. Additionally, its application extends to materials science, where it aids in the development of advanced polymers and catalysts with specific stereochemical properties.
| 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 | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :