(S)-4-Benzyloxazolidine-2-thione
≥98%,≥99% e.e.
- Product Code: 62507
CAS:
145588-94-9
| Molecular Weight: | 193.3 g./mol | Molecular Formula: | C₁₀H₁₁NOS |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 63-67°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
(S)-4-Benzyloxazolidine-2-thione is primarily utilized in organic synthesis as a chiral auxiliary and building block for the preparation of enantiomerically pure compounds. It plays a significant role in asymmetric synthesis, particularly in the formation of chiral intermediates for pharmaceuticals and bioactive molecules. Its structure is advantageous in controlling stereochemistry during reactions, making it valuable in the synthesis of complex organic molecules. Additionally, it is employed in the development of catalysts and ligands for asymmetric catalysis, enhancing the efficiency and selectivity of chemical transformations. Its applications extend to research in medicinal chemistry, where it aids in the creation of chiral drugs and therapeutic agents.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Off white or beige powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,860.00 |
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| 1.000 | 10-20 days | ฿10,080.00 |
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(S)-4-Benzyloxazolidine-2-thione
(S)-4-Benzyloxazolidine-2-thione is primarily utilized in organic synthesis as a chiral auxiliary and building block for the preparation of enantiomerically pure compounds. It plays a significant role in asymmetric synthesis, particularly in the formation of chiral intermediates for pharmaceuticals and bioactive molecules. Its structure is advantageous in controlling stereochemistry during reactions, making it valuable in the synthesis of complex organic molecules. Additionally, it is employed in the development of catalysts and ligands for asymmetric catalysis, enhancing the efficiency and selectivity of chemical transformations. Its applications extend to research in medicinal chemistry, where it aids in the creation of chiral drugs and therapeutic agents.
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