3-(N,N-Diethylaminocarbonyl)phenylboronic acid pinacol ester
95%
- Product Code: 83538
CAS:
325142-97-0
| Molecular Weight: | 303.20 g./mol | Molecular Formula: | C₁₇H₂₆BNO₃ |
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| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester functionality ensures stability and reactivity, making it suitable for use in mild reaction conditions. Additionally, it finds applications in the development of sensors and molecular probes due to its ability to interact with diols and other biologically relevant molecules. Its role in medicinal chemistry is significant, as it aids in the synthesis of drug candidates and bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,611.00 |
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| 5.000 | 10-20 days | ฿7,191.00 |
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3-(N,N-Diethylaminocarbonyl)phenylboronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester functionality ensures stability and reactivity, making it suitable for use in mild reaction conditions. Additionally, it finds applications in the development of sensors and molecular probes due to its ability to interact with diols and other biologically relevant molecules. Its role in medicinal chemistry is significant, as it aids in the synthesis of drug candidates and bioactive compounds.
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