(R)-Diphenylprolinol Trimethyl Silyl Ether
≥95%,99%e.e.
- Product Code: 70398
CAS:
943757-71-9
| Molecular Weight: | 325.5 g./mol | Molecular Formula: | C₂₀H₂₇NOSi |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | 1.406g/mL | Storage Condition: | room temperature, dry |
Product Description:
(R)-Diphenylprolinol Trimethyl Silyl Ether is widely used as a chiral catalyst in asymmetric synthesis, particularly in organic reactions such as aldol reactions, Michael additions, and cycloadditions. Its ability to induce high enantioselectivity makes it valuable in the production of pharmaceuticals, where the creation of specific stereoisomers is crucial for drug efficacy and safety. Additionally, it is employed in the synthesis of complex natural products and fine chemicals, enabling the development of compounds with precise stereochemical configurations. Its stability and reactivity under mild conditions further enhance its utility in laboratory and industrial settings.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Yellow or White to Tan Solid or Liquid |
| PURITY | 95-100 |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿780.00 |
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| 1.000 | 10-20 days | ฿2,660.00 |
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| 5.000 | 10-20 days | ฿9,390.00 |
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(R)-Diphenylprolinol Trimethyl Silyl Ether
(R)-Diphenylprolinol Trimethyl Silyl Ether is widely used as a chiral catalyst in asymmetric synthesis, particularly in organic reactions such as aldol reactions, Michael additions, and cycloadditions. Its ability to induce high enantioselectivity makes it valuable in the production of pharmaceuticals, where the creation of specific stereoisomers is crucial for drug efficacy and safety. Additionally, it is employed in the synthesis of complex natural products and fine chemicals, enabling the development of compounds with precise stereochemical configurations. Its stability and reactivity under mild conditions further enhance its utility in laboratory and industrial settings.
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