3-Fluoro-4-(morpholinomethyl)phenylboronic acid
98%
- Product Code: 90154
CAS:
1333388-00-3
| Molecular Weight: | 239.06 g./mol | Molecular Formula: | C₁₁H₁₅BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16198064 | |
| 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. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The morpholinomethyl substituent enhances solubility and stability, facilitating its use in complex molecular transformations. It is often employed in the development of bioactive molecules and drug intermediates, contributing to the synthesis of compounds with potential therapeutic applications. Additionally, its fluorine atom can influence the electronic properties of the resulting products, making it useful in designing molecules with specific reactivity or biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $1,133.77 |
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3-Fluoro-4-(morpholinomethyl)phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The morpholinomethyl substituent enhances solubility and stability, facilitating its use in complex molecular transformations. It is often employed in the development of bioactive molecules and drug intermediates, contributing to the synthesis of compounds with potential therapeutic applications. Additionally, its fluorine atom can influence the electronic properties of the resulting products, making it useful in designing molecules with specific reactivity or biological activity.
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