(S)-4-Benzyl-2-(thiophen-2-yl)-4,5-dihydrooxazole
97%
- Product Code: 38542
CAS:
149065-75-8
| Molecular Weight: | 243.32 g./mol | Molecular Formula: | C₁₄H₁₃NOS |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. Its structure, featuring a benzyl group and a thiophene ring, enhances its ability to induce stereoselectivity in reactions such as hydrogenation, carbon-carbon bond formation, and cycloaddition processes. Additionally, it is employed in the development of novel catalysts for organic transformations, contributing to more efficient and sustainable chemical processes. Its application extends to research in material science, where it aids in the synthesis of chiral polymers and advanced materials with specific optical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,815.00 |
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(S)-4-Benzyl-2-(thiophen-2-yl)-4,5-dihydrooxazole
This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. Its structure, featuring a benzyl group and a thiophene ring, enhances its ability to induce stereoselectivity in reactions such as hydrogenation, carbon-carbon bond formation, and cycloaddition processes. Additionally, it is employed in the development of novel catalysts for organic transformations, contributing to more efficient and sustainable chemical processes. Its application extends to research in material science, where it aids in the synthesis of chiral polymers and advanced materials with specific optical properties.
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