(S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidine
97%
- Product Code: 38376
CAS:
207113-36-8
| Molecular Weight: | 201.3812 g./mol | Molecular Formula: | C₁₀H₂₃NOSi |
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| EC Number: | MDL Number: | MFCD09909497 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
(S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidine is widely used in organic synthesis, particularly as a chiral building block or intermediate in the production of pharmaceuticals and bioactive compounds. Its silyl-protected hydroxyl group enhances stability and selectivity during complex reactions, making it valuable in asymmetric synthesis. This compound is often employed in the development of drugs targeting neurological disorders, such as antidepressants and antipsychotics, due to its pyrrolidine structure, which is a common motif in CNS-active molecules. Additionally, it serves as a key reagent in the synthesis of natural products and peptidomimetics, where precise stereochemistry is crucial for biological activity. Its role in protecting group chemistry also facilitates the stepwise construction of complex molecules in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿6,255.00 |
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(S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidine
(S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidine is widely used in organic synthesis, particularly as a chiral building block or intermediate in the production of pharmaceuticals and bioactive compounds. Its silyl-protected hydroxyl group enhances stability and selectivity during complex reactions, making it valuable in asymmetric synthesis. This compound is often employed in the development of drugs targeting neurological disorders, such as antidepressants and antipsychotics, due to its pyrrolidine structure, which is a common motif in CNS-active molecules. Additionally, it serves as a key reagent in the synthesis of natural products and peptidomimetics, where precise stereochemistry is crucial for biological activity. Its role in protecting group chemistry also facilitates the stepwise construction of complex molecules in medicinal chemistry research.
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