(R)-4-Phenyl-2-(2-((S)-p-tolylsulfinyl)phenyl)-4,5-dihydrooxazole
98%
- Product Code: 231350
CAS:
2509221-06-9
| Molecular Weight: | 361.46 g./mol | Molecular Formula: | C₂₂H₁₉NO₂S |
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| Density: | Storage Condition: | 2-8°C, light-proof, inert gas |
Product Description:
Used as a chiral auxiliary or ligand in asymmetric synthesis, particularly in enantioselective catalysis. Its rigid oxazole framework and stereogenic centers make it effective in controlling stereochemistry during carbon-carbon bond-forming reactions. Commonly employed in asymmetric aldol, Diels-Alder, and Michael addition reactions to achieve high enantiomeric excess. The sulfinyl group enhances coordination with metal centers, enabling efficient chiral induction when used in metal-catalyzed transformations. Also applied in the synthesis of pharmaceutical intermediates where precise stereocontrol is required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿12,160.00 |
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| 250mg | 10-20 days | ฿20,960.00 |
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| 1g | 10-20 days | ฿70,660.00 |
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(R)-4-Phenyl-2-(2-((S)-p-tolylsulfinyl)phenyl)-4,5-dihydrooxazole
Used as a chiral auxiliary or ligand in asymmetric synthesis, particularly in enantioselective catalysis. Its rigid oxazole framework and stereogenic centers make it effective in controlling stereochemistry during carbon-carbon bond-forming reactions. Commonly employed in asymmetric aldol, Diels-Alder, and Michael addition reactions to achieve high enantiomeric excess. The sulfinyl group enhances coordination with metal centers, enabling efficient chiral induction when used in metal-catalyzed transformations. Also applied in the synthesis of pharmaceutical intermediates where precise stereocontrol is required.
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