2-Fluoro-4-(1-pyrrolidinylcarbonyl)benzeneboronic acid
95%
- Product Code: 67380
CAS:
874289-25-5
| Molecular Weight: | 237.0352232 g./mol | Molecular Formula: | C₁₁H₁₃BFNO₃ |
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| EC Number: | MDL Number: | MFCD16036548 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of aryl groups into various organic molecules, enabling the creation of complex structures in pharmaceuticals, agrochemicals, and materials science. Its boronic acid functional group facilitates efficient and selective coupling with aryl halides or triflates, making it valuable in the development of active pharmaceutical ingredients (APIs) and advanced materials. Additionally, its pyrrolidinylcarbonyl moiety can enhance solubility and stability, broadening its applicability in diverse synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿5,850.00 |
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| 0.250 | 10-20 days | ฿23,382.00 |
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2-Fluoro-4-(1-pyrrolidinylcarbonyl)benzeneboronic acid
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of aryl groups into various organic molecules, enabling the creation of complex structures in pharmaceuticals, agrochemicals, and materials science. Its boronic acid functional group facilitates efficient and selective coupling with aryl halides or triflates, making it valuable in the development of active pharmaceutical ingredients (APIs) and advanced materials. Additionally, its pyrrolidinylcarbonyl moiety can enhance solubility and stability, broadening its applicability in diverse synthetic pathways.
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