3-Quinolineboronic acid pinacol ester
95%
- Product Code: 90132
Alias:
3-Quinolineboronic acid pinacol ester
Quinoline-3-boronic acid pinacol ester
CAS:
171364-85-5
| Molecular Weight: | 255.12 g./mol | Molecular Formula: | C₁₅H₁₈BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05155218 | |
| Melting Point: | 56-60 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound facilitates the synthesis of complex organic molecules, particularly in pharmaceutical research. It is employed in the development of drug candidates, enabling the formation of carbon-carbon bonds in a controlled manner. Additionally, it serves as a building block in the creation of advanced materials, such as organic semiconductors and light-emitting diodes (LEDs), due to its ability to introduce quinoline moieties into larger structures. Its stability and reactivity make it a valuable tool in medicinal chemistry and material science applications.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 95 100% |
| APPEARANCE | White to off-white powder or solid or chunks |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿920.00 |
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| 5.000 | 10-20 days | ฿2,760.00 |
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| 25.000 | 10-20 days | ฿12,980.00 |
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3-Quinolineboronic acid pinacol ester
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound facilitates the synthesis of complex organic molecules, particularly in pharmaceutical research. It is employed in the development of drug candidates, enabling the formation of carbon-carbon bonds in a controlled manner. Additionally, it serves as a building block in the creation of advanced materials, such as organic semiconductors and light-emitting diodes (LEDs), due to its ability to introduce quinoline moieties into larger structures. Its stability and reactivity make it a valuable tool in medicinal chemistry and material science applications.
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