(5-Fluoro-6-methoxypyridin-3-yl)boronic Acid
98%, containing different amounts of acid anhydride
- Product Code: 64167
CAS:
856250-60-7
| Molecular Weight: | 170.93 g./mol | Molecular Formula: | C₆H₇BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04112520 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
(5-Fluoro-6-methoxypyridin-3-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is a key method for forming carbon-carbon bonds, making the compound valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the creation of complex organic molecules. Additionally, it is employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to introduce specific functional groups into molecular frameworks. Its stability and reactivity make it a versatile reagent in medicinal chemistry and material science research.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Almost white Crystal - Powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿2,250.00 |
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| 1.000 | 10-20 days | ฿6,620.00 |
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| 5.000 | 10-20 days | ฿23,130.00 |
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(5-Fluoro-6-methoxypyridin-3-yl)boronic Acid
(5-Fluoro-6-methoxypyridin-3-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is a key method for forming carbon-carbon bonds, making the compound valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the creation of complex organic molecules. Additionally, it is employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to introduce specific functional groups into molecular frameworks. Its stability and reactivity make it a versatile reagent in medicinal chemistry and material science research.
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