Ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate
≥95%
- Product Code: 192609
CAS:
1256360-06-1
| Molecular Weight: | 265.11 g./mol | Molecular Formula: | C₁₃H₂₀BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16036144 | |
| Melting Point: | Boiling Point: | 364.3±34.0 °C(Predicted) | |
| Density: | 1.08±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing complex pyrrole-containing molecules. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The ethyl carboxylate group adds stability and can be further modified, allowing for diverse derivatization pathways. It is especially useful in the development of bioactive compounds, functional materials, and heterocyclic systems where pyrrole motifs are essential.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿2,900.00 |
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| 0.250 G | 10-20 days | ฿4,990.00 |
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| 1.000 G | 10-20 days | ฿13,300.00 |
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Ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing complex pyrrole-containing molecules. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The ethyl carboxylate group adds stability and can be further modified, allowing for diverse derivatization pathways. It is especially useful in the development of bioactive compounds, functional materials, and heterocyclic systems where pyrrole motifs are essential.
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