(3-Chloro-2-fluorophenyl)boronic acid
97%
- Product Code: 90195
CAS:
352535-82-1
| Molecular Weight: | 174.37 g./mol | Molecular Formula: | C₆H₅BClFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 223°C | Boiling Point: | 315.1°C |
| Density: | Storage Condition: | 2-8°C |
Product Description:
(3-Chloro-2-fluorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in drug discovery and development. Additionally, it is employed in the synthesis of biologically active compounds and in the modification of organic frameworks for material science applications. Its stability and reactivity make it a versatile reagent in both academic research and industrial processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿540.00 |
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| 5.000 | 10-20 days | ฿1,780.00 |
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| 25.000 | 10-20 days | ฿6,450.00 |
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| 100.000 | 10-20 days | ฿19,800.00 |
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(3-Chloro-2-fluorophenyl)boronic acid
(3-Chloro-2-fluorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in drug discovery and development. Additionally, it is employed in the synthesis of biologically active compounds and in the modification of organic frameworks for material science applications. Its stability and reactivity make it a versatile reagent in both academic research and industrial processes.
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