3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole
98%
- Product Code: 83716
CAS:
214360-77-7
| Molecular Weight: | 193.05 g./mol | Molecular Formula: | C₁₀H₁₆BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11109266 | |
| Melting Point: | 77-79 °C | Boiling Point: | 310.947 °C(Predicted) |
| Density: | 1.04 g/cm3(Predicted) | Storage Condition: | -20°C, inert gas |
Product Description:
This chemical is widely utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. Additionally, it is employed in the synthesis of heterocyclic compounds, which are essential in drug discovery and material science. Its stability and reactivity make it a preferred choice for researchers working on advanced organic transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,294.00 |
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| 1.000 | 10-20 days | ฿8,901.00 |
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| 5.000 | 10-20 days | ฿32,058.00 |
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3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole
This chemical is widely utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. Additionally, it is employed in the synthesis of heterocyclic compounds, which are essential in drug discovery and material science. Its stability and reactivity make it a preferred choice for researchers working on advanced organic transformations.
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