4-((tert-Butoxycarbonyl(cyclopropyl)amino)methyl)-3-fluorophenylboronic aci
98%
- Product Code: 90316
CAS:
1704064-03-8
Molecular Weight: | 309.15 g./mol | Molecular Formula: | C₁₅H₂₁BFNO₄ |
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EC Number: | MDL Number: | MFCD28400168 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables it to act as a key intermediate in forming carbon-carbon bonds, which is essential in constructing complex organic molecules. The cyclopropyl and tert-butoxycarbonyl groups provide steric and electronic effects that can influence the reactivity and selectivity of the compound in these reactions. It is often employed in the development of pharmaceuticals and agrochemicals, where precise molecular architecture is critical. Additionally, the fluorine atom can enhance the metabolic stability and bioavailability of the resulting compounds, making it valuable in drug discovery and medicinal chemistry applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $1,336.01 |
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4-((tert-Butoxycarbonyl(cyclopropyl)amino)methyl)-3-fluorophenylboronic aci
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables it to act as a key intermediate in forming carbon-carbon bonds, which is essential in constructing complex organic molecules. The cyclopropyl and tert-butoxycarbonyl groups provide steric and electronic effects that can influence the reactivity and selectivity of the compound in these reactions. It is often employed in the development of pharmaceuticals and agrochemicals, where precise molecular architecture is critical. Additionally, the fluorine atom can enhance the metabolic stability and bioavailability of the resulting compounds, making it valuable in drug discovery and medicinal chemistry applications.
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