(2-(tert-butyl)cyclopropyl)boronic acid
95%
- Product Code: 89018
CAS:
680600-46-8
| Molecular Weight: | 142.0038 g./mol | Molecular Formula: | C₇H₁₅BO₂ |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
(2-(tert-butyl)cyclopropyl)boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. This reaction is widely employed in the pharmaceutical and materials science industries to construct complex organic molecules, including drug candidates and advanced polymers. The compound serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds with high efficiency and selectivity. Its unique cyclopropyl structure, combined with the tert-butyl group, can impart steric and electronic effects that influence the reactivity and stability of the intermediates formed during the reaction. Additionally, it may be used in the development of biologically active compounds, where the cyclopropyl moiety can enhance metabolic stability or modulate the pharmacological properties of the target molecule. Its application extends to the synthesis of agrochemicals and fine chemicals, where precise control over molecular architecture is essential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿78,000.00 |
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-
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| 0.100 | 10-20 days | ฿230,000.00 |
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(2-(tert-butyl)cyclopropyl)boronic acid
(2-(tert-butyl)cyclopropyl)boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. This reaction is widely employed in the pharmaceutical and materials science industries to construct complex organic molecules, including drug candidates and advanced polymers. The compound serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds with high efficiency and selectivity. Its unique cyclopropyl structure, combined with the tert-butyl group, can impart steric and electronic effects that influence the reactivity and stability of the intermediates formed during the reaction. Additionally, it may be used in the development of biologically active compounds, where the cyclopropyl moiety can enhance metabolic stability or modulate the pharmacological properties of the target molecule. Its application extends to the synthesis of agrochemicals and fine chemicals, where precise control over molecular architecture is essential.
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