Ethyl 1-(3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)Cyclopropane-1-Carboxylate
97%
- Product Code: 185592
CAS:
1521255-61-7
| Molecular Weight: | 316.2 g./mol | Molecular Formula: | C₁₈H₂₅BO₄ |
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| Density: | Storage Condition: | Room temperature |
Product Description:
Used primarily as an 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 substituted aromatic and cyclopropane-containing structures. The ethyl ester functionality allows further transformations, such as hydrolysis to the corresponding carboxylic acid or use in peptide-like coupling reactions. Its stability and reactivity profile make it suitable for late-stage functionalization in drug discovery and materials science.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿2,040.00 |
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| 0.250 G | 10-20 days | ฿4,880.00 |
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Ethyl 1-(3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)Cyclopropane-1-Carboxylate
Used primarily as an 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 substituted aromatic and cyclopropane-containing structures. The ethyl ester functionality allows further transformations, such as hydrolysis to the corresponding carboxylic acid or use in peptide-like coupling reactions. Its stability and reactivity profile make it suitable for late-stage functionalization in drug discovery and materials science.
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