(S)-4-Phenyl-2-(pyridin-2-ylmethyl)-4,5-dihydrooxazole
97%
- Product Code: 236576
CAS:
404844-76-4
| Molecular Weight: | 238.28 g./mol | Molecular Formula: | C₁₅H₁₄N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD34563691 | |
| Melting Point: | Boiling Point: | 386.8±42.0 °C(Predicted) | |
| Density: | 1.16±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, inert gas |
Product Description:
Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its oxazoline core with a pyridine substituent enables coordination to metal centers, making it effective in catalyzing reactions such as asymmetric allylic alkylation and Diels-Alder reactions. The compound is valued for its ability to induce high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals. It is also employed in the development of novel ligands for transition metal-catalyzed transformations, where stereocontrol is critical.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,540.00 |
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| 0.250 | 10-20 days | ฿6,050.00 |
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| 1.000 | 10-20 days | ฿22,770.00 |
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(S)-4-Phenyl-2-(pyridin-2-ylmethyl)-4,5-dihydrooxazole
Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its oxazoline core with a pyridine substituent enables coordination to metal centers, making it effective in catalyzing reactions such as asymmetric allylic alkylation and Diels-Alder reactions. The compound is valued for its ability to induce high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals. It is also employed in the development of novel ligands for transition metal-catalyzed transformations, where stereocontrol is critical.
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