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CAS 855230-61-4

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3-Ethoxy-2-fluorophenylboronic acid

Description:
3-Ethoxy-2-fluorophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a fluorine atom and an ethoxy group attached to a phenyl ring, contributing to its unique reactivity and solubility properties. Typically, boronic acids are polar and can exhibit moderate solubility in polar solvents, while the presence of the ethoxy group may enhance its solubility in organic solvents. This compound is often utilized in medicinal chemistry and materials science for the synthesis of complex organic molecules. Additionally, the fluorine substituent can influence the electronic properties of the molecule, potentially affecting its reactivity and interactions in biological systems. As with many boronic acids, it is important to handle this compound with care, as it may be sensitive to moisture and air, which can affect its stability and reactivity.
Formula:C8H10BFO3
InChI:InChI=1S/C8H10BFO3/c1-2-13-7-5-3-4-6(8(7)10)9(11)12/h3-5,11-12H,2H2,1H3
InChI key:InChIKey=DCUXBPVUKGENEJ-UHFFFAOYSA-N
SMILES:O(CC)C1=C(F)C(B(O)O)=CC=C1
Synonyms:
  • 3-Ethoxy-2-fluorophenylboronic acid
  • B-(3-Ethoxy-2-fluorophenyl)boronic acid
  • Boronic acid, (3-ethoxy-2-fluorophenyl)-
  • boronic acid, B-(3-ethoxy-2-fluorophenyl)-
  • (3-Ethoxy-2-fluorophenyl)boronic acid
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