N-Cyclopentyl 4-borono-2-fluorobenzamide
95%
- Product Code: 60846
CAS:
957034-70-7
| Molecular Weight: | 251.06 g./mol | Molecular Formula: | C₁₂H₁₅BFNO₃ |
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| EC Number: | MDL Number: | MFCD09475825 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key boron-containing reagent. Its structure, featuring a boronic acid group, enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The fluorine substituent enhances its reactivity and selectivity in these reactions, allowing for more precise control over the final product. Additionally, its cyclopentyl moiety can influence the steric and electronic properties, further optimizing its performance in catalytic processes. This compound is often employed in the development of drug candidates, where its ability to introduce aromatic rings with specific functional groups is crucial for achieving desired biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿2,637.00 |
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| 0.250 | 10-20 days | ฿7,848.00 |
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| 1.000 | 10-20 days | ฿28,350.00 |
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N-Cyclopentyl 4-borono-2-fluorobenzamide
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key boron-containing reagent. Its structure, featuring a boronic acid group, enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The fluorine substituent enhances its reactivity and selectivity in these reactions, allowing for more precise control over the final product. Additionally, its cyclopentyl moiety can influence the steric and electronic properties, further optimizing its performance in catalytic processes. This compound is often employed in the development of drug candidates, where its ability to introduce aromatic rings with specific functional groups is crucial for achieving desired biological activity.
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