2,3-Difluoro-6-methoxyphenylboronic acid
98%
- Product Code: 89895
CAS:
957061-21-1
| Molecular Weight: | 187.94 g./mol | Molecular Formula: | C₇H₇BF₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03095116 | |
| Melting Point: | Boiling Point: | 322.4°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the construction of biaryl structures. Additionally, it is employed in the development of materials for electronic devices, such as organic light-emitting diodes (OLEDs), due to its ability to modify the electronic properties of conjugated systems. Its fluorine and methoxy substituents further enhance its reactivity and selectivity in various chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | ฿432.00 |
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| 1.000 | 10-20 days | ฿1,116.00 |
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2,3-Difluoro-6-methoxyphenylboronic acid
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the construction of biaryl structures. Additionally, it is employed in the development of materials for electronic devices, such as organic light-emitting diodes (OLEDs), due to its ability to modify the electronic properties of conjugated systems. Its fluorine and methoxy substituents further enhance its reactivity and selectivity in various chemical transformations.
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