Tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-pyrrole-1-carboxylate
95%
- Product Code: 242052
CAS:
1401165-14-7
| Molecular Weight: | 295.18 g./mol | Molecular Formula: | C₁₅H₂₆BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16996221 | |
| Melting Point: | Boiling Point: | 321.9 °C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a versatile boronate ester reagent. It enables the formation of carbon-carbon bonds by reacting with aryl or vinyl halides under palladium catalysis, making it valuable in the construction of complex organic molecules. Its protected dihydropyrrole structure is useful in medicinal chemistry for developing nitrogen-containing heterocycles found in bioactive compounds and pharmaceuticals. The tert-butyl carbamate (Boc) group provides stability and allows for selective deprotection, facilitating stepwise synthesis in multi-step reaction sequences. Commonly employed in the development of drug candidates and functional materials, it supports efficient and selective transformations in both academic and industrial research settings.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | $13.75 |
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| 0.025 | 10-20 days | $31.77 |
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Tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-pyrrole-1-carboxylate
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a versatile boronate ester reagent. It enables the formation of carbon-carbon bonds by reacting with aryl or vinyl halides under palladium catalysis, making it valuable in the construction of complex organic molecules. Its protected dihydropyrrole structure is useful in medicinal chemistry for developing nitrogen-containing heterocycles found in bioactive compounds and pharmaceuticals. The tert-butyl carbamate (Boc) group provides stability and allows for selective deprotection, facilitating stepwise synthesis in multi-step reaction sequences. Commonly employed in the development of drug candidates and functional materials, it supports efficient and selective transformations in both academic and industrial research settings.
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