N-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2-methoxyacetamide
95%
- Product Code: 83835
CAS:
2246668-24-4
| Molecular Weight: | 309.1409 g./mol | Molecular Formula: | C₁₅H₂₁BFNO₄ |
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| EC Number: | MDL Number: | MFCD32206465 | |
| Melting Point: | Boiling Point: | ||
| Density: | 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 boronate ester group acts as a key functional moiety, enabling the formation of carbon-carbon bonds, which is essential in the development of pharmaceuticals, agrochemicals, and advanced materials. The presence of the fluorine atom enhances its reactivity and selectivity, making it a valuable intermediate in the synthesis of complex molecules. Additionally, the methoxyacetamide group can contribute to the compound's solubility and stability, facilitating its use in various chemical processes. Its applications are particularly significant in medicinal chemistry, where it is employed to create biologically active compounds with potential therapeutic effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | $261.91 |
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| 0.100 | 10-20 days | $787.15 |
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N-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2-methoxyacetamide
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group acts as a key functional moiety, enabling the formation of carbon-carbon bonds, which is essential in the development of pharmaceuticals, agrochemicals, and advanced materials. The presence of the fluorine atom enhances its reactivity and selectivity, making it a valuable intermediate in the synthesis of complex molecules. Additionally, the methoxyacetamide group can contribute to the compound's solubility and stability, facilitating its use in various chemical processes. Its applications are particularly significant in medicinal chemistry, where it is employed to create biologically active compounds with potential therapeutic effects.
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