rel-Ethyl(1R,2S)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopropane-1-carboxylate
98%
- Product Code: 186019
CAS:
2135443-14-8
| Molecular Weight: | 240.10 g./mol | Molecular Formula: | C₁₂H₂₁BO₄ |
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| EC Number: | MDL Number: | MFCD32066801 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling 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 for constructing cyclopropane-containing structures. The ethyl ester functionality allows for further synthetic manipulation, such as hydrolysis or reduction, to access a range of functionalized cyclopropane derivatives important in bioactive compound development.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 100mg | 10-20 days | $690.51 |
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| 250mg | 10-20 days | $1,047.16 |
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| 500mg | 10-20 days | $1,634.33 |
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| 1g | 10-20 days | $2,127.71 |
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rel-Ethyl(1R,2S)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopropane-1-carboxylate
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling 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 for constructing cyclopropane-containing structures. The ethyl ester functionality allows for further synthetic manipulation, such as hydrolysis or reduction, to access a range of functionalized cyclopropane derivatives important in bioactive compound development.
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