tert-butyl 3-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)pyrrolidine-1-carboxylate
90%
- Product Code: 242151
CAS:
2365173-49-3
| Molecular Weight: | 309.21 g./mol | Molecular Formula: | C₁₆H₂₈BNO₄ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
Used primarily as a building block in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The tert-butyl carbamate-protected pyrrolidine moiety allows for further functionalization of nitrogen-containing heterocycles, commonly found in bioactive compounds. It is especially useful in medicinal chemistry for constructing drug-like scaffolds and optimizing lead compounds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿17,150.00 |
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| 1.000 | 10-20 days | ฿28,560.00 |
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tert-butyl 3-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)pyrrolidine-1-carboxylate
Used primarily as a building block in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The tert-butyl carbamate-protected pyrrolidine moiety allows for further functionalization of nitrogen-containing heterocycles, commonly found in bioactive compounds. It is especially useful in medicinal chemistry for constructing drug-like scaffolds and optimizing lead compounds.
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