Shi Epoxidation Diketal Catalyst
98%
- Product Code: 58029
CAS:
18422-53-2
| Molecular Weight: | 258.27 g./mol | Molecular Formula: | C₁₂H₁₈O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00063383 | |
| Melting Point: | 102-104°C (Lit.) | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
The Shi epoxidation diketal catalyst is widely used in organic synthesis for the enantioselective epoxidation of alkenes. This catalyst is particularly valuable in the production of chiral epoxides, which are important intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to selectively oxidize alkenes to epoxides with high enantiomeric excess makes it a crucial tool in asymmetric synthesis. The catalyst is often employed in the development of drugs, where the stereochemistry of the molecules plays a critical role in their biological activity. Additionally, it is used in academic research to explore new synthetic pathways and to study the mechanisms of asymmetric catalysis.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White crystalline powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿4,260.00 |
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| 5.000 | 10-20 days | ฿10,800.00 |
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| 25.000 | 10-20 days | ฿42,850.00 |
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Shi Epoxidation Diketal Catalyst
The Shi epoxidation diketal catalyst is widely used in organic synthesis for the enantioselective epoxidation of alkenes. This catalyst is particularly valuable in the production of chiral epoxides, which are important intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to selectively oxidize alkenes to epoxides with high enantiomeric excess makes it a crucial tool in asymmetric synthesis. The catalyst is often employed in the development of drugs, where the stereochemistry of the molecules plays a critical role in their biological activity. Additionally, it is used in academic research to explore new synthetic pathways and to study the mechanisms of asymmetric catalysis.
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