(S)-2-(thiophen-2-yl)-4-phenyl-4,5-dihydrooxazole
95%
- Product Code: 236255
CAS:
149065-77-0
| Molecular Weight: | 229.30 g./mol | Molecular Formula: | C₁₃H₁₁NOS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31802358 | |
| Melting Point: | Boiling Point: | 383.1±35.0 °C(Predicted) | |
| Density: | 1.25±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature |
Product Description:
Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the development of enantiomerically pure pharmaceuticals. Its oxazoline ring provides a rigid framework that facilitates stereocontrol in reactions such as alkylations, aldol additions, and cycloadditions. Commonly employed in coordination with metal catalysts to induce chirality in carbon-carbon bond-forming reactions. Also utilized in the synthesis of bioactive molecules where stereoselectivity is critical, including natural products and drug candidates. The thiophene and phenyl groups enhance ligand binding and influence electronic properties in catalytic systems.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,720.00 |
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| 250mg | 10-20 days | ฿4,940.00 |
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| 1g | 10-20 days | ฿9,880.00 |
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(S)-2-(thiophen-2-yl)-4-phenyl-4,5-dihydrooxazole
Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the development of enantiomerically pure pharmaceuticals. Its oxazoline ring provides a rigid framework that facilitates stereocontrol in reactions such as alkylations, aldol additions, and cycloadditions. Commonly employed in coordination with metal catalysts to induce chirality in carbon-carbon bond-forming reactions. Also utilized in the synthesis of bioactive molecules where stereoselectivity is critical, including natural products and drug candidates. The thiophene and phenyl groups enhance ligand binding and influence electronic properties in catalytic systems.
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