3-Fluorophenylboronic acid

97%

  • Product Code: 90183
  Alias:    3-fluorophenylboronic acid; 3-fluorophenylboronic acid, m-fluorophenylboronic acid
  CAS:    768-35-4
Molecular Weight: 139.92 g./mol Molecular Formula: C₆H₆BFO₂
EC Number: MDL Number: MFCD00236042
Melting Point: 214-218 °C(lit.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: 3-Fluorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of various biologically active molecules, including drug candidates targeting cancer, inflammation, and infectious diseases. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and other functional groups, making it useful in glucose sensing and other analytical applications. Its versatility and reactivity make it a crucial component in modern chemical research and industrial processes.
Product Specification:
Test Specification
Purity 97 100%
APPEARANCE WHITE TO OFF-WHITE POWDER OR CRYSTALS
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿320.00
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5.000 10-20 days ฿570.00
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25.000 10-20 days ฿1,160.00
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-
100.000 10-20 days ฿3,920.00
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-
500.000 10-20 days ฿19,470.00
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3-Fluorophenylboronic acid
3-Fluorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of various biologically active molecules, including drug candidates targeting cancer, inflammation, and infectious diseases. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and other functional groups, making it useful in glucose sensing and other analytical applications. Its versatility and reactivity make it a crucial component in modern chemical research and industrial processes.
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