Tert-butyl 3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-yl)pyrrolidine-1-carboxylate
95%
- Product Code: 242068
CAS:
2223006-81-1
| Molecular Weight: | 363.2562 g./mol | Molecular Formula: | C₁₉H₃₀BNO₅ |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
Used primarily as an intermediate in pharmaceutical synthesis, this compound plays a key role in Suzuki-Miyaura cross-coupling reactions, where the boronate ester group enables the formation of carbon-carbon bonds. Its structure supports the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in the development of drug candidates, especially in medicinal chemistry for CNS-targeted therapies and kinase inhibitors. The tert-butyl carbamate (Boc) protecting group ensures stability and controlled reactivity of the pyrrolidine nitrogen during multi-step syntheses. Its furan and pyrrolidine motifs are valuable for building molecular diversity in high-throughput drug discovery.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25mg | 10-20 days | ฿87,040.00 |
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| 100mg | 10-20 days | ฿256,630.00 |
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Tert-butyl 3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-yl)pyrrolidine-1-carboxylate
Used primarily as an intermediate in pharmaceutical synthesis, this compound plays a key role in Suzuki-Miyaura cross-coupling reactions, where the boronate ester group enables the formation of carbon-carbon bonds. Its structure supports the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in the development of drug candidates, especially in medicinal chemistry for CNS-targeted therapies and kinase inhibitors. The tert-butyl carbamate (Boc) protecting group ensures stability and controlled reactivity of the pyrrolidine nitrogen during multi-step syntheses. Its furan and pyrrolidine motifs are valuable for building molecular diversity in high-throughput drug discovery.
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