4-Carboxy-3-fluorophenylboronic acid
98%
- Product Code: 90722
Alias:
4-Carboxy-3-fluorophenylboronic acid
3-fluoro-4-carboxyphenylboronic acid
CAS:
120153-08-4
Molecular Weight: | 183.93 g./mol | Molecular Formula: | C₇H₆BFO₄ |
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EC Number: | MDL Number: | MFCD01114671 | |
Melting Point: | 236-240°C | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
This chemical is primarily used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. It is often employed in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, due to the presence of the boronic acid group. The fluorine substituent can enhance the stability and reactivity of the molecule, making it valuable in the development of drug candidates or materials with specific properties. Additionally, its carboxylic acid group allows for further functionalization, enabling its use in creating complex molecular structures. This compound is also explored in research for potential applications in medicinal chemistry, such as enzyme inhibitors or receptor-targeting molecules.
Product Specification:
Test | Specification |
---|---|
Melting point | 236-240 |
PURITYHPLC | 98-100 |
APPEARANCE | White to off-white solid |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿470.00 |
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5.000 | 10-20 days | ฿1,980.00 |
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25.000 | 10-20 days | ฿9,100.00 |
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4-Carboxy-3-fluorophenylboronic acid
This chemical is primarily used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. It is often employed in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, due to the presence of the boronic acid group. The fluorine substituent can enhance the stability and reactivity of the molecule, making it valuable in the development of drug candidates or materials with specific properties. Additionally, its carboxylic acid group allows for further functionalization, enabling its use in creating complex molecular structures. This compound is also explored in research for potential applications in medicinal chemistry, such as enzyme inhibitors or receptor-targeting molecules.
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