5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isothiazole
98%
- Product Code: 131872
CAS:
1045809-78-6
| Molecular Weight: | 211.09 g./mol | Molecular Formula: | C₉H₁₄BNO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08061126 | |
| Melting Point: | Boiling Point: | 234.4±22.0 °C(Predicted) | |
| Density: | 1.12±0.1 g/cm3(Predicted) | Storage Condition: | -20°C, Sealed, Dry |
Product Description:
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing for the formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in medicinal chemistry for constructing biaryl systems found in bioactive molecules. It is also employed in the development of functional materials, including organic semiconductors and ligands for catalysts, due to the stability and reactivity of the isothiazole ring combined with the versatility of the boronate functionality.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $359.63 |
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| 0.250 | 10-20 days | $612.18 |
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| 1.000 | 10-20 days | $1,592.04 |
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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isothiazole
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing for the formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in medicinal chemistry for constructing biaryl systems found in bioactive molecules. It is also employed in the development of functional materials, including organic semiconductors and ligands for catalysts, due to the stability and reactivity of the isothiazole ring combined with the versatility of the boronate functionality.
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