ethyl 4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)cyclohexane-1-carboxylate
95%
- Product Code: 184006
CAS:
2365173-46-0
| Molecular Weight: | 294.2 g./mol | Molecular Formula: | C₁₆H₂₇BO₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry, stored away from light |
Product Description:
Used primarily as a building block 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 readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The ester functionality allows for further derivatization, such as hydrolysis or reduction, enabling diverse molecular transformations. Its structure supports the creation of substituted cyclohexyl derivatives, which are common motifs in bioactive compounds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿4,150.00 |
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| 5g | 10-20 days | ฿67,500.00 |
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| bulk | 10-20 days | ฿0.00 |
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| 1g | 10-20 days | ฿28,800.00 |
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ethyl 4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)cyclohexane-1-carboxylate
Used primarily as a building block 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 readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The ester functionality allows for further derivatization, such as hydrolysis or reduction, enabling diverse molecular transformations. Its structure supports the creation of substituted cyclohexyl derivatives, which are common motifs in bioactive compounds.
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