3-Chloro-5-fluorobenzeneboronic acid
98%
- Product Code: 90215
Alias:
3-Chloro-5-fluorophenylboronic acid
CAS:
328956-61-2
| Molecular Weight: | 174.37 g./mol | Molecular Formula: | C₆H₅BClFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06801741 | |
| Melting Point: | >200°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic compounds, especially in the pharmaceutical industry. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of various biologically active molecules. It is also employed in the development of agrochemicals and materials science, where it contributes to the creation of advanced polymers and functional materials. Its halogen substituents enhance reactivity and selectivity in coupling reactions, making it a valuable reagent in medicinal chemistry for drug discovery and development.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98-100 |
| APPEARANCE | White to off white Crystal |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿560.00 |
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| 5.000 | 10-20 days | ฿2,700.00 |
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| 25.000 | 10-20 days | ฿11,630.00 |
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3-Chloro-5-fluorobenzeneboronic acid
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic compounds, especially in the pharmaceutical industry. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of various biologically active molecules. It is also employed in the development of agrochemicals and materials science, where it contributes to the creation of advanced polymers and functional materials. Its halogen substituents enhance reactivity and selectivity in coupling reactions, making it a valuable reagent in medicinal chemistry for drug discovery and development.
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