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CAS 849062-29-9

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B-(5-Chloro-2-propoxyphenyl)boronic acid

Description:
B-(5-Chloro-2-propoxyphenyl)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, 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 propoxy group enhances its lipophilicity, potentially affecting its biological activity and interaction with other molecules. Typically, boronic acids are utilized in organic synthesis, medicinal chemistry, and materials science due to their versatility. The presence of the chlorine atom may also impart specific electronic properties, affecting the compound's reactivity. Additionally, the compound's solubility in organic solvents and its stability under various conditions are important characteristics that determine its practical applications. Overall, B-(5-Chloro-2-propoxyphenyl)boronic acid is a valuable building block in synthetic chemistry, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C9H12BClO3
InChI:InChI=1S/C9H12BClO3/c1-2-5-14-9-4-3-7(11)6-8(9)10(12)13/h3-4,6,12-13H,2,5H2,1H3
InChI key:InChIKey=FZDSWPMDXOYUBB-UHFFFAOYSA-N
SMILES:O(CCC)C1=C(B(O)O)C=C(Cl)C=C1
Synonyms:
  • Boronic acid, (5-chloro-2-propoxyphenyl)-
  • Boronic acid, B-(5-chloro-2-propoxyphenyl)-
  • B-(5-Chloro-2-propoxyphenyl)boronic acid
  • 5-Chloro-2-propoxyphenylboronic acid
  • See more synonyms
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