(2-Fluoro-6-methylphenyl)boronic acid
95%
- Product Code: 89044
CAS:
887471-69-4
| Molecular Weight: | 153.95 g./mol | Molecular Formula: | C₇H₈BFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13194360 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
(2-Fluoro-6-methylphenyl)boronic 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. Its specific structure allows for selective coupling with various aryl halides, enabling the synthesis of complex organic molecules. Additionally, it serves as a key intermediate in the development of bioactive compounds and drug candidates, particularly in medicinal chemistry research. Its stability and reactivity make it a preferred choice for constructing diverse aromatic systems in industrial and laboratory settings.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-white Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,930.00 |
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| 0.250 | 10-20 days | ฿3,540.00 |
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| 1.000 | 10-20 days | ฿10,450.00 |
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(2-Fluoro-6-methylphenyl)boronic acid
(2-Fluoro-6-methylphenyl)boronic 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. Its specific structure allows for selective coupling with various aryl halides, enabling the synthesis of complex organic molecules. Additionally, it serves as a key intermediate in the development of bioactive compounds and drug candidates, particularly in medicinal chemistry research. Its stability and reactivity make it a preferred choice for constructing diverse aromatic systems in industrial and laboratory settings.
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