7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]isothiazole
97%
- Product Code: 238160
CAS:
1326713-92-1
| Molecular Weight: | 261.15 g./mol | Molecular Formula: | C₁₃H₁₆BNO₂S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 326.6±24.0 °C(Predicted) | |
| Density: | 1.17±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or heteroaryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the benzoisothiazole moiety into target structures, which is a common scaffold in bioactive compounds and functional materials. Its stability and reactivity profile make it suitable for late-stage functionalization in drug discovery and development.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿16,350.00 |
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| 1.000 | 10-20 days | ฿75,010.00 |
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7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]isothiazole
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or heteroaryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the benzoisothiazole moiety into target structures, which is a common scaffold in bioactive compounds and functional materials. Its stability and reactivity profile make it suitable for late-stage functionalization in drug discovery and development.
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