6-Quinolineboronic acid pinacol ester
≥98%
- Product Code: 90950
CAS:
406463-06-7
| Molecular Weight: | 255.13 g./mol | Molecular Formula: | C₁₅H₁₈BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06411327 | |
| Melting Point: | 62-66ºC | Boiling Point: | 386.5ºC |
| Density: | 1.1g/cm3 | Storage Condition: | room temperature, dry |
Product Description:
6-Quinolineboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it suitable for creating quinoline derivatives, which are often found in drugs targeting various diseases, including cancer and infectious diseases. Additionally, it is employed in the development of organic electronic materials, such as light-emitting diodes (LEDs) and semiconductors, due to its ability to introduce functional groups into aromatic systems.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 98-100 |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,890.00 |
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| 5.000 | 10-20 days | ฿7,120.00 |
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6-Quinolineboronic acid pinacol ester
6-Quinolineboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it suitable for creating quinoline derivatives, which are often found in drugs targeting various diseases, including cancer and infectious diseases. Additionally, it is employed in the development of organic electronic materials, such as light-emitting diodes (LEDs) and semiconductors, due to its ability to introduce functional groups into aromatic systems.
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