(5-Phenoxypyridin-3-yl)boronic acid
97%
- Product Code: 89359
CAS:
850991-33-2
| Molecular Weight: | 215.01 g./mol | Molecular Formula: | C₁₁H₁₀BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09907982 | |
| Melting Point: | Boiling Point: | 419.3 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical research for creating drug intermediates. Additionally, it finds application in material science for developing organic electronic materials and polymers. Its stability and reactivity make it a versatile tool in synthetic chemistry for designing molecules with specific properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,229.00 |
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| 0.250 | 10-20 days | ฿8,694.00 |
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| 1.000 | 10-20 days | ฿17,388.00 |
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(5-Phenoxypyridin-3-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical research for creating drug intermediates. Additionally, it finds application in material science for developing organic electronic materials and polymers. Its stability and reactivity make it a versatile tool in synthetic chemistry for designing molecules with specific properties.
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