(3-((3-fluorophenyl)carbamoyl)phenyl)boronic acid
98%
- Product Code: 89099
CAS:
874288-34-3
| Molecular Weight: | 259.04 g./mol | Molecular Formula: | C₁₃H₁₁BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09027207 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.34g/mL | 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 group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the fluorophenyl group can enhance the compound's reactivity and selectivity in these reactions. Additionally, it may be used in the development of bioactive molecules or as an intermediate in the synthesis of compounds with potential therapeutic applications. Its unique structure allows for precise modifications in drug design and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,140.00 |
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(3-((3-fluorophenyl)carbamoyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the fluorophenyl group can enhance the compound's reactivity and selectivity in these reactions. Additionally, it may be used in the development of bioactive molecules or as an intermediate in the synthesis of compounds with potential therapeutic applications. Its unique structure allows for precise modifications in drug design and material science.
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