4-Fluoro-2-(trifluoromethyl)benzeneboronic acid
98%
- Product Code: 90591
Alias:
4-Fluoro-2-trifluoromethylphenylboronic acid
CAS:
182344-16-7
| Molecular Weight: | 207.92 g./mol | Molecular Formula: | C₇H₅BF₄O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08062379 | |
| Melting Point: | 183-186°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex aromatic compounds, which are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl structures that are often found in active pharmaceutical ingredients (APIs). Additionally, it is employed in the preparation of fluorinated organic compounds, which are valuable in medicinal chemistry due to their enhanced metabolic stability and bioavailability. The compound’s trifluoromethyl group further contributes to its utility in creating molecules with unique electronic and steric properties, making it a versatile tool in drug discovery and material science.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 183 186? |
| PURITYHPLC | 98 100% |
| 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 |
|---|---|---|---|
| 0.250 | 10-20 days | ฿330.00 |
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| 1.000 | 10-20 days | ฿410.00 |
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| 5.000 | 10-20 days | ฿1,300.00 |
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| 25.000 | 10-20 days | ฿5,330.00 |
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4-Fluoro-2-(trifluoromethyl)benzeneboronic acid
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex aromatic compounds, which are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl structures that are often found in active pharmaceutical ingredients (APIs). Additionally, it is employed in the preparation of fluorinated organic compounds, which are valuable in medicinal chemistry due to their enhanced metabolic stability and bioavailability. The compound’s trifluoromethyl group further contributes to its utility in creating molecules with unique electronic and steric properties, making it a versatile tool in drug discovery and material science.
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