(S)-tert-Butyl 3-((methylsulfonyl)oxy)pyrrolidine-1-carboxylate
97%
- Product Code: 235035
CAS:
132945-75-6
| Molecular Weight: | 265.33 g./mol | Molecular Formula: | C₁₀H₁₉NO₅S |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its activated leaving group (methylsulfonyloxy) enables efficient alkylation or ring-opening reactions, making it valuable for constructing complex nitrogen-containing molecules. Commonly employed in asymmetric synthesis to introduce the (S)-pyrrolidine scaffold, which is prevalent in drug candidates targeting central nervous system disorders, antiviral agents, and enzyme inhibitors. The tert-butyl carbamate (Boc) protection allows for selective deprotection under mild acidic conditions, enabling stepwise assembly in multi-step organic syntheses.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 1g | 10-20 days | €16.87 |
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| 5g | 10-20 days | €80.90 |
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| 25g | 10-20 days | €349.18 |
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(S)-tert-Butyl 3-((methylsulfonyl)oxy)pyrrolidine-1-carboxylate
Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its activated leaving group (methylsulfonyloxy) enables efficient alkylation or ring-opening reactions, making it valuable for constructing complex nitrogen-containing molecules. Commonly employed in asymmetric synthesis to introduce the (S)-pyrrolidine scaffold, which is prevalent in drug candidates targeting central nervous system disorders, antiviral agents, and enzyme inhibitors. The tert-butyl carbamate (Boc) protection allows for selective deprotection under mild acidic conditions, enabling stepwise assembly in multi-step organic syntheses.
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