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
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
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
1.000 10-20 days ฿670.00
+
-
5.000 10-20 days ฿1,880.00
+
-
25.000 10-20 days ฿8,260.00
+
-
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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