(2R)-2-[Bis[3,5-bis(trifluoromethyl)phenyl]-[(tert-butyldimethylsilyl)oxy]methyl]pyrrolidine
≥98%,99%e.e.
- Product Code: 70412
CAS:
1146629-74-4
| Molecular Weight: | 639.6 g./mol | Molecular Formula: | C₂₇H₂₉F₁₂NOSi |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized as a chiral ligand or catalyst in asymmetric synthesis, particularly in organic reactions where high enantioselectivity is required. It is often employed in the development of pharmaceuticals and fine chemicals, where controlling the stereochemistry of the product is crucial. Its unique structure, featuring trifluoromethyl groups and a silyl-protected hydroxyl, enhances its stability and reactivity in complex catalytic processes. Additionally, it is used in the synthesis of biologically active compounds, aiding in the creation of enantiomerically pure substances for drug discovery and development. Its application extends to academic research, where it serves as a valuable tool for studying stereoselective transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,494.00 |
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(2R)-2-[Bis[3,5-bis(trifluoromethyl)phenyl]-[(tert-butyldimethylsilyl)oxy]methyl]pyrrolidine
This chemical is primarily utilized as a chiral ligand or catalyst in asymmetric synthesis, particularly in organic reactions where high enantioselectivity is required. It is often employed in the development of pharmaceuticals and fine chemicals, where controlling the stereochemistry of the product is crucial. Its unique structure, featuring trifluoromethyl groups and a silyl-protected hydroxyl, enhances its stability and reactivity in complex catalytic processes. Additionally, it is used in the synthesis of biologically active compounds, aiding in the creation of enantiomerically pure substances for drug discovery and development. Its application extends to academic research, where it serves as a valuable tool for studying stereoselective transformations.
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