(2-(Methoxymethyl)phenyl)boronic acid
97%
- Product Code: 89855
CAS:
126617-98-9
| Molecular Weight: | 165.98 g./mol | Molecular Formula: | C₈H₁₁BO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03412110 | |
| Melting Point: | 42-44°C | Boiling Point: | 309.8°C |
| Density: | Storage Condition: | 2-8°C |
Product Description:
(2-(Methoxymethyl)phenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling of aryl or vinyl halides with aryl or vinyl boronic acids. Additionally, it finds applications in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it valuable in biochemical and analytical research. Its stability and reactivity also make it a preferred choice in medicinal chemistry for drug discovery and development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿315.00 |
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| 1.000 | 10-20 days | ฿684.00 |
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| 5.000 | 10-20 days | ฿3,087.00 |
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(2-(Methoxymethyl)phenyl)boronic acid
(2-(Methoxymethyl)phenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling of aryl or vinyl halides with aryl or vinyl boronic acids. Additionally, it finds applications in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it valuable in biochemical and analytical research. Its stability and reactivity also make it a preferred choice in medicinal chemistry for drug discovery and development processes.
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