2-Chloro-4-pyridylboronic acid
95%
- Product Code: 89772
Alias:
2-Chloro-4-pyridineboronic acid
CAS:
458532-96-2
| Molecular Weight: | 157.36 g./mol | Molecular Formula: | C₅H₅ClNO₂B |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03788416 | |
| Melting Point: | 155-163 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for creating complex molecules, including pharmaceuticals and agrochemicals. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in constructing pyridine-containing compounds. Additionally, it is employed in the development of materials for electronic devices and organic light-emitting diodes (OLEDs) due to its ability to modify and enhance molecular structures. Its applications also extend to research in medicinal chemistry, where it aids in the synthesis of biologically active compounds.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 155-163 |
| Purity | 95-100 |
| APPEARANCE | White to tan powder,crystals and/or chunks |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿520.00 |
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| 5.000 | 10-20 days | ฿1,530.00 |
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| 25.000 | 10-20 days | ฿6,950.00 |
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2-Chloro-4-pyridylboronic acid
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for creating complex molecules, including pharmaceuticals and agrochemicals. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in constructing pyridine-containing compounds. Additionally, it is employed in the development of materials for electronic devices and organic light-emitting diodes (OLEDs) due to its ability to modify and enhance molecular structures. Its applications also extend to research in medicinal chemistry, where it aids in the synthesis of biologically active compounds.
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