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CAS 1256355-63-1

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B-[4-(2-Fluoroethoxy)phenyl]boronic acid

Description:
B-[4-(2-Fluoroethoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a 2-fluoroethoxy group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the fluorinated ethoxy group can enhance its solubility and reactivity, potentially influencing its interactions in biological systems. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds in organic synthesis. The compound's structure suggests it may have applications in drug development or as a building block in the synthesis of more complex molecules. Its specific reactivity and stability would depend on the surrounding conditions, such as pH and the presence of other functional groups.
Formula:C8H10BFO3
InChI:InChI=1S/C8H10BFO3/c10-5-6-13-8-3-1-7(2-4-8)9(11)12/h1-4,11-12H,5-6H2
InChI key:InChIKey=XNKMLDGLDSQHSH-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC=C(OCCF)C=C1
Synonyms:
  • [4-(2-Fluoroethoxy)phenyl]boronic acid
  • Boronic acid, B-[4-(2-fluoroethoxy)phenyl]-
  • B-[4-(2-Fluoroethoxy)phenyl]boronic acid
  • 4-(2-Fluoroethoxy)phenylboronic acid
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