4-(2-(Di(adamantan-1-yl)phosphino)phenyl)morpholine
98%
- Product Code: 68332
CAS:
1237588-12-3
| Molecular Weight: | 463.63 g./mol | Molecular Formula: | C₃₀H₄₂NOP |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17018759 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Inert gas, 2-8°C |
Product Description:
This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its unique structure, featuring adamantyl groups and a morpholine moiety, enhances stability and selectivity in various catalytic applications. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Additionally, its steric and electronic properties make it suitable for asymmetric catalysis, contributing to the synthesis of chiral molecules in pharmaceuticals and fine chemicals. The ligand’s robustness under harsh reaction conditions further expands its utility in industrial and academic research settings.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $161.13 |
+
-
|
| 0.250 | 10-20 days | $285.72 |
+
-
|
| 1.000 | 10-20 days | $1,071.45 |
+
-
|
4-(2-(Di(adamantan-1-yl)phosphino)phenyl)morpholine
This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its unique structure, featuring adamantyl groups and a morpholine moiety, enhances stability and selectivity in various catalytic applications. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Additionally, its steric and electronic properties make it suitable for asymmetric catalysis, contributing to the synthesis of chiral molecules in pharmaceuticals and fine chemicals. The ligand’s robustness under harsh reaction conditions further expands its utility in industrial and academic research settings.
| 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 :