4-Fluoro-2-((4-methylpiperidin-1-yl)methyl)phenylboronic acid
98%
- Product Code: 90586
CAS:
1704063-82-0
| Molecular Weight: | 251.11 g./mol | Molecular Formula: | C₁₃H₁₉BFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400162 | |
| 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. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. The boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in active pharmaceutical ingredients. Its fluorine substituent can enhance the stability and reactivity of the resulting compounds, making it valuable in drug discovery and development. Additionally, the piperidine moiety may contribute to the compound's ability to interact with biological targets, potentially aiding in the design of bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿17,100.00 |
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4-Fluoro-2-((4-methylpiperidin-1-yl)methyl)phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. The boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in active pharmaceutical ingredients. Its fluorine substituent can enhance the stability and reactivity of the resulting compounds, making it valuable in drug discovery and development. Additionally, the piperidine moiety may contribute to the compound's ability to interact with biological targets, potentially aiding in the design of bioactive molecules.
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