2,6-Bis[(4R)-4-tert-butyloxazolin-2-yl]pyridine
≥98%,99%e.e.
- Product Code: 70600
CAS:
185346-17-2
| Molecular Weight: | 329.4 g./mol | Molecular Formula: | C₁₉H₂₇N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized as a ligand in asymmetric catalysis, particularly in the synthesis of chiral compounds. Its structure, featuring oxazoline rings, makes it effective in coordinating with transition metals like palladium, platinum, and rhodium. This coordination enables the formation of highly active catalysts used in enantioselective reactions, such as hydrogenation, allylic alkylation, and cross-coupling reactions. These processes are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals, where achieving a specific enantiomer is essential for the desired biological activity. Additionally, its sterically demanding tert-butyl groups enhance selectivity and stability in catalytic systems, making it a valuable tool in organic synthesis.
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 |
|---|---|---|---|
| 0.500 | 10-20 days | ฿4,990.00 |
+
-
|
2,6-Bis[(4R)-4-tert-butyloxazolin-2-yl]pyridine
This chemical is primarily utilized as a ligand in asymmetric catalysis, particularly in the synthesis of chiral compounds. Its structure, featuring oxazoline rings, makes it effective in coordinating with transition metals like palladium, platinum, and rhodium. This coordination enables the formation of highly active catalysts used in enantioselective reactions, such as hydrogenation, allylic alkylation, and cross-coupling reactions. These processes are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals, where achieving a specific enantiomer is essential for the desired biological activity. Additionally, its sterically demanding tert-butyl groups enhance selectivity and stability in catalytic systems, making it a valuable tool in organic synthesis.
| 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 :