Tert-butyl 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazol-2-yl)pyrrolidine-1-carboxylate
95%
- Product Code: 242054
CAS:
2222995-74-4
| Molecular Weight: | 380.30986 g./mol | Molecular Formula: | C₁₈H₂₉BN₂O₄S |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. The boronate ester group facilitates coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable for constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for the synthesis of bioactive molecules, particularly those containing thiazole and pyrrolidine motifs. Its protected amine group allows for further functionalization after coupling, offering versatility in multi-step synthetic routes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿53,110.00 |
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| 0.100 | 10-20 days | ฿159,320.00 |
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Tert-butyl 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazol-2-yl)pyrrolidine-1-carboxylate
Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. The boronate ester group facilitates coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable for constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for the synthesis of bioactive molecules, particularly those containing thiazole and pyrrolidine motifs. Its protected amine group allows for further functionalization after coupling, offering versatility in multi-step synthetic routes.
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