3,5-Dimethylisoxazole-4-boronic acid
97%
- Product Code: 89937
Alias:
3,5-Dimethylisoxazole-4-boronic acid
CAS:
16114-47-9
| Molecular Weight: | 140.93 g./mol | Molecular Formula: | C₅H₈BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02677945 | |
| Melting Point: | 108-113 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
3,5-Dimethylisoxazole-4-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 the compound valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional moiety, enabling the coupling with various aryl or vinyl halides in the presence of a palladium catalyst. This versatility allows for the creation of complex molecules with potential applications in drug discovery, where it can be used to synthesize bioactive compounds or intermediates. Additionally, it finds utility in materials science for designing organic electronic components or polymers with tailored properties. The compound’s stability and reactivity make it a preferred choice in modern synthetic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 106-108 |
| PURITY TITRATION BY NAOH | 96.5-103.5 |
| PURITYHPLC | 97-100 |
| APPEARANCE | WHITE TO YELLOW TO BROWN POWDER,CRYSTALS OR CHUNKS |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿1,040.00 |
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| 25.000 | 10-20 days | ฿4,190.00 |
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| 100.000 | 10-20 days | ฿16,550.00 |
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3,5-Dimethylisoxazole-4-boronic acid
3,5-Dimethylisoxazole-4-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 the compound valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional moiety, enabling the coupling with various aryl or vinyl halides in the presence of a palladium catalyst. This versatility allows for the creation of complex molecules with potential applications in drug discovery, where it can be used to synthesize bioactive compounds or intermediates. Additionally, it finds utility in materials science for designing organic electronic components or polymers with tailored properties. The compound’s stability and reactivity make it a preferred choice in modern synthetic chemistry.
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