3-Carboxy-4-fluorophenylboronic acid
97%
- Product Code: 90271
Alias:
3-Carboxy-4-fluorophenylboronic acid
CAS:
872460-12-3
Molecular Weight: | 183.93 g./mol | Molecular Formula: | C₇H₆BFO₄ |
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EC Number: | MDL Number: | ||
Melting Point: | 217-219°C | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
This compound is primarily utilized in organic synthesis and medicinal chemistry as a versatile building block. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds, which is essential in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The fluorine substituent enhances its reactivity and selectivity in these reactions, making it valuable for creating complex molecules. Additionally, it is employed in the development of boron-based drugs and as a precursor for sensors and probes in biochemical research due to its ability to interact with diols and other biological targets.
Product Specification:
Test | Specification |
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LOSS ON DRYING | 0-0.5 |
PURITYLC | 97-100 |
HEAVY METALSAS PB | 0-0.002 |
IRONFE | 0-0.005 |
Appearance | Off-white powder |
SOLUBILITY IN AMMONIA WATER | almost transparency |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿670.00 |
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5.000 | 10-20 days | ฿1,880.00 |
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25.000 | 10-20 days | ฿8,260.00 |
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3-Carboxy-4-fluorophenylboronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry as a versatile building block. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds, which is essential in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The fluorine substituent enhances its reactivity and selectivity in these reactions, making it valuable for creating complex molecules. Additionally, it is employed in the development of boron-based drugs and as a precursor for sensors and probes in biochemical research due to its ability to interact with diols and other biological targets.
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