3-Fluoro-4-formylphenylboronic acid

98%

  • Product Code: 90163
  Alias:    3-Fluoro-4-formylphenylboronic acid
  CAS:    248270-25-9
Molecular Weight: 167.93 g./mol Molecular Formula: C₇H₆BFO₃
EC Number: MDL Number: MFCD02093051
Melting Point: 249-250°C Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex molecules. Its boronic acid group facilitates the coupling with aryl halides, making it valuable in drug discovery and development. Additionally, it is employed in the synthesis of fluorescent probes and sensors due to its ability to interact with specific biological targets. Its formyl group allows for further functionalization, enhancing its versatility in designing advanced materials and bioactive compounds.
Product Specification:
Test Specification
PURITYNEUTRALIZATION TITRATION 97.5 102.5%
APPEARANCE WHITE TO TAN POWDER CRYSTALS AND/OR CHUNKS
INFRARED SPECTRUM Conforms to Structure
PROTON NMR SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $44.62
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5.000 10-20 days $193.02
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25.000 10-20 days $775.85
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3-Fluoro-4-formylphenylboronic acid
Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex molecules. Its boronic acid group facilitates the coupling with aryl halides, making it valuable in drug discovery and development. Additionally, it is employed in the synthesis of fluorescent probes and sensors due to its ability to interact with specific biological targets. Its formyl group allows for further functionalization, enhancing its versatility in designing advanced materials and bioactive compounds.
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