3,5-Dimethylisoxazole-4-boronic acid pinacol ester
98%
- Product Code: 89939
CAS:
832114-00-8
| Molecular Weight: | 223.08 g./mol | Molecular Formula: | C₁₁H₁₈BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05863910 | |
| Melting Point: | 95-99 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of the 3,5-dimethylisoxazole moiety into more complex molecules. Its boronic ester group facilitates efficient coupling with various aryl or vinyl halides, enabling the construction of carbon-carbon bonds. This makes it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its stability and reactivity under mild conditions make it a preferred choice for researchers working on drug discovery and functional molecule design.
Product Specification:
| Test | Specification |
|---|---|
| CARBON | 57.2-61.3 |
| Melting point | 96-101 |
| NITROGEN | 6-6.5 |
| PURITY GC | 98-100 |
| APPEARANCE | White to yellow to beige Powder or crystals |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿360.00 |
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| 5.000 | 10-20 days | ฿910.00 |
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| 25.000 | 10-20 days | ฿3,820.00 |
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3,5-Dimethylisoxazole-4-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of the 3,5-dimethylisoxazole moiety into more complex molecules. Its boronic ester group facilitates efficient coupling with various aryl or vinyl halides, enabling the construction of carbon-carbon bonds. This makes it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its stability and reactivity under mild conditions make it a preferred choice for researchers working on drug discovery and functional molecule design.
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