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CAS 279261-81-3

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3-Chloro-4-ethoxyphenylboronic acid

Description:
3-Chloro-4-ethoxyphenylboronic 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. This compound features a chlorinated aromatic ring, which can influence its reactivity and solubility. The ethoxy group enhances its lipophilicity, potentially improving its bioavailability in pharmaceutical applications. Typically, boronic acids like this one are utilized in organic synthesis, medicinal chemistry, and materials science due to their versatile reactivity. The presence of the chlorine atom can also impart unique electronic properties, affecting the compound's overall stability and reactivity. In terms of physical properties, it is likely to be a solid at room temperature, with solubility in polar organic solvents. Safety data should be consulted for handling, as boronic acids can pose hazards if not managed properly. Overall, 3-Chloro-4-ethoxyphenylboronic acid is a valuable compound in synthetic organic chemistry.
Formula:C8H10BClO3
InChI:InChI=1S/C8H10BClO3/c1-2-13-8-4-3-6(9(11)12)5-7(8)10/h3-5,11-12H,2H2,1H3
InChI key:InChIKey=QZMQZKMQXURQNC-UHFFFAOYSA-N
SMILES:O(CC)C1=C(Cl)C=C(B(O)O)C=C1
Synonyms:
  • (3-Chloro-4-ethoxyphenyl)boronic acid
  • 3-Chloro-4-Ethoxybenzeneboronic Acid
  • B-(3-Chloro-4-ethoxyphenyl)boronic acid
  • Boronic acid, (3-chloro-4-ethoxyphenyl)-
  • Boronic acid, B-(3-chloro-4-ethoxyphenyl)-
  • 3-Chloro-4-ethoxyphenylboronic acid
  • 3-Chloro-4-Ethoxyphenylboronic
  • 3-CHLORO-4-ERHOXYPHENYLBONIC ACID
  • 3-Chloro-4-ethoxypheylboronic acid
  • AKOS BRN-0596
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