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CAS 957062-68-9

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2-Ethoxy-6-fluorophenylboronic acid

Description:
2-Ethoxy-6-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 applications, particularly in organic synthesis and medicinal chemistry. The compound features a fluorine atom substituted at the 6-position of a phenyl ring, which can influence its electronic properties and reactivity. The ethoxy group at the 2-position enhances its solubility in organic solvents and may affect its interaction with biological targets. This compound is typically used in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the presence of the boronic acid moiety allows for potential applications in drug development and materials science. Its stability, reactivity, and functionalization potential make it a valuable building block in synthetic organic chemistry. Safety data should be reviewed before handling, as with all chemical substances, to ensure proper precautions are taken.
Formula:C8H10BFO3
InChI:InChI=1/C8H10BFO3/c1-2-13-7-5-3-4-6(10)8(7)9(11)12/h3-5,11-12H,2H2,1H3
SMILES:CCOc1cccc(c1B(O)O)F
Synonyms:
  • (2-Ethoxy-6-fluorophenyl)boronic acid
  • boronic acid, B-(2-ethoxy-6-fluorophenyl)-
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