(4-(3-Fluorophenoxy)phenyl)boronic acid
98%
- Product Code: 118559
CAS:
1029438-36-5
| Molecular Weight: | 232.02 g./mol | Molecular Formula: | C₁₂H₁₀BFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14636485 | |
| Melting Point: | Boiling Point: | 373.7±52.0 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient formation of carbon-carbon bonds, making it valuable in synthesizing compounds with potential biological activity. Additionally, it may be employed in material science for designing advanced polymers or functional materials. Its fluorophenoxy moiety can enhance the stability and specificity of the resulting compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $39.96 |
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| 0.250 | 10-20 days | $60.22 |
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| 1.000 | 10-20 days | $226.82 |
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(4-(3-Fluorophenoxy)phenyl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient formation of carbon-carbon bonds, making it valuable in synthesizing compounds with potential biological activity. Additionally, it may be employed in material science for designing advanced polymers or functional materials. Its fluorophenoxy moiety can enhance the stability and specificity of the resulting compounds.
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