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CAS 2096334-30-2

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B-(3-Chloro-4-ethoxy-5-fluorophenyl)boronic acid

Description:
B-(3-Chloro-4-ethoxy-5-fluorophenyl)boronic 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 and other nucleophiles. This compound features a phenyl ring substituted with a chlorine atom, an ethoxy group, and a fluorine atom, contributing to its unique reactivity and potential applications in medicinal chemistry and organic synthesis. The presence of the boronic acid moiety allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, making it valuable in the synthesis of complex organic molecules. Additionally, the halogen and ethoxy substituents can influence the compound's solubility, stability, and biological activity. As with many boronic acids, it may exhibit sensitivity to moisture and air, necessitating careful handling and storage conditions. Overall, this compound's structural features suggest potential utility in drug development and materials science.
Formula:C8H9BClFO3
InChI:InChI=1S/C8H9BClFO3/c1-2-14-8-6(10)3-5(9(12)13)4-7(8)11/h3-4,12-13H,2H2,1H3
InChI key:InChIKey=AAPPGBQQZJDSBE-UHFFFAOYSA-N
SMILES:O(CC)C1=C(Cl)C=C(B(O)O)C=C1F
Synonyms:
  • Boronic acid, B-(3-chloro-4-ethoxy-5-fluorophenyl)-
  • B-(3-Chloro-4-ethoxy-5-fluorophenyl)boronic acid
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