5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-inden-2-ol
98%
- Product Code: 243421
CAS:
1857348-77-6
| Molecular Weight: | 260.14 g./mol | Molecular Formula: | C₁₅H₂₁BO₃ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used primarily as a key intermediate 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 is highly effective in palladium-catalyzed couplings, making it valuable in pharmaceutical and agrochemical research for constructing biaryl and heterobiaryl systems. The presence of the hydroxyl group allows for further functionalization or use in directed ortho-metalation strategies. It is especially useful in medicinal chemistry for building constrained cyclic frameworks found in bioactive compounds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿12,480.00 |
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| 0.100 | 10-20 days | ฿19,200.00 |
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| 0.250 | 10-20 days | ฿33,600.00 |
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| 1.000 | 10-20 days | ฿92,800.00 |
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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-inden-2-ol
Used primarily as a key intermediate 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 is highly effective in palladium-catalyzed couplings, making it valuable in pharmaceutical and agrochemical research for constructing biaryl and heterobiaryl systems. The presence of the hydroxyl group allows for further functionalization or use in directed ortho-metalation strategies. It is especially useful in medicinal chemistry for building constrained cyclic frameworks found in bioactive compounds.
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