4-Fluoro-3-methoxybenzeneboronic acid
97%
- Product Code: 90605
Alias:
4-fluoro-3-methoxyphenylboronic acid
CAS:
854778-31-7
| Molecular Weight: | 169.95 g./mol | Molecular Formula: | C₇H₈BFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08056358 | |
| Melting Point: | 189-191 | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
4-Fluoro-3-methoxybenzeneboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key building block in the synthesis of complex organic molecules, including drug candidates and biologically active compounds. Its boronic acid group enables efficient coupling with aryl halides, while the fluorine and methoxy substituents can influence the reactivity and stability of the resulting products. Additionally, it is utilized in the development of sensors and catalysts due to its unique electronic properties.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 189 191? |
| PURITYHPLC | 97 100% |
| APPEARANCE | White to off-white powder or solid or chunks |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿330.00 |
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| 1.000 | 10-20 days | ฿610.00 |
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| 5.000 | 10-20 days | ฿2,820.00 |
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| 25.000 | 10-20 days | ฿11,820.00 |
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4-Fluoro-3-methoxybenzeneboronic acid
4-Fluoro-3-methoxybenzeneboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key building block in the synthesis of complex organic molecules, including drug candidates and biologically active compounds. Its boronic acid group enables efficient coupling with aryl halides, while the fluorine and methoxy substituents can influence the reactivity and stability of the resulting products. Additionally, it is utilized in the development of sensors and catalysts due to its unique electronic properties.
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