(R)-4-Isopropyl-2-oxazolidinethione
≥95%,≥99%e.e.
- Product Code: 62482
CAS:
1217463-35-8
| Molecular Weight: | 145.2 g./mol | Molecular Formula: | C₆H₁₁NOS |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 48-52°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a chiral auxiliary, enabling the production of enantiomerically pure substances. It plays a crucial role in asymmetric synthesis, particularly in the formation of complex molecules with high stereochemical control. Its application is significant in the pharmaceutical industry, where it aids in the development of chiral drugs, ensuring the desired enantiomer is produced for enhanced efficacy and reduced side effects. Additionally, it is employed in academic research for studying stereoselective reactions and developing new synthetic methodologies.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | pale yellow powder |
| PURITY | 95-100 |
| Infrared spectrum | Conforms to Structure |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,395.00 |
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| 1.000 | 10-20 days | ฿3,951.00 |
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| 5.000 | 10-20 days | ฿18,486.00 |
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(R)-4-Isopropyl-2-oxazolidinethione
This compound is primarily utilized in organic synthesis as a chiral auxiliary, enabling the production of enantiomerically pure substances. It plays a crucial role in asymmetric synthesis, particularly in the formation of complex molecules with high stereochemical control. Its application is significant in the pharmaceutical industry, where it aids in the development of chiral drugs, ensuring the desired enantiomer is produced for enhanced efficacy and reduced side effects. Additionally, it is employed in academic research for studying stereoselective reactions and developing new synthetic methodologies.
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