2-Fluoro-3-methoxyphenylboronic acid
97%
- Product Code: 67369
Alias:
2-fluoro-3-methoxyphenylboronic acid
CAS:
352303-67-4
| Molecular Weight: | 169.95 g./mol | Molecular Formula: | C₇H₈BFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02094728 | |
| Melting Point: | 117-122 °C(lit.) | Boiling Point: | 326.8ºC at 760 mmHg |
| Density: | 1.26g/cm3 | Storage Condition: | room temperature |
Product Description:
Widely used in Suzuki-Miyaura cross-coupling reactions to synthesize complex biaryl compounds, which are essential in pharmaceutical and agrochemical industries. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs), particularly in the development of drugs targeting neurological and oncological diseases. Additionally, it is employed in material science for creating advanced organic electronic materials, such as OLEDs and organic semiconductors, due to its ability to introduce specific functional groups into molecular structures. Its unique boronic acid group also makes it valuable in sensor development for detecting sugars and other biomolecules.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97 100% |
| Melting point | 117 125? |
| LOSS ON DRYING | 0.5 |
| APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿500.00 |
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| 25.000 | 10-20 days | ฿2,400.00 |
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| 100.000 | 10-20 days | ฿9,290.00 |
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2-Fluoro-3-methoxyphenylboronic acid
Widely used in Suzuki-Miyaura cross-coupling reactions to synthesize complex biaryl compounds, which are essential in pharmaceutical and agrochemical industries. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs), particularly in the development of drugs targeting neurological and oncological diseases. Additionally, it is employed in material science for creating advanced organic electronic materials, such as OLEDs and organic semiconductors, due to its ability to introduce specific functional groups into molecular structures. Its unique boronic acid group also makes it valuable in sensor development for detecting sugars and other biomolecules.
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