Phenyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrol-1-yl)methanone
95%
- Product Code: 192606
CAS:
1256360-12-9
| Molecular Weight: | 297.16 g./mol | Molecular Formula: | C₁₇H₂₀BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16036151 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronate ester group reacts efficiently with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable for constructing complex aromatic and heteroaromatic systems. Commonly employed in pharmaceutical and agrochemical research for building functionalized pyrrole derivatives, which are important scaffolds in bioactive molecules. The compound’s stability and reactivity profile make it suitable for use in both academic and industrial settings, especially in drug discovery and materials science.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿6,000.00 |
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| 0.250 G | 10-20 days | ฿10,240.00 |
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| 1.000 G | 10-20 days | ฿26,600.00 |
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Phenyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrol-1-yl)methanone
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronate ester group reacts efficiently with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable for constructing complex aromatic and heteroaromatic systems. Commonly employed in pharmaceutical and agrochemical research for building functionalized pyrrole derivatives, which are important scaffolds in bioactive molecules. The compound’s stability and reactivity profile make it suitable for use in both academic and industrial settings, especially in drug discovery and materials science.
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