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CAS 352534-86-2

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5-Chloro-2-ethoxyphenylboronic acid

Description:
5-Chloro-2-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. The compound features a chloro substituent at the 5-position and an ethoxy group at the 2-position of a phenyl ring, contributing to its unique reactivity and solubility properties. Typically, boronic acids like this one are polar and can exhibit moderate solubility in polar solvents, while their reactivity allows them to participate in cross-coupling reactions, which are essential in organic synthesis for forming carbon-carbon bonds. The presence of the chloro and ethoxy groups can influence the electronic properties of the molecule, affecting its reactivity and interaction with other chemical species. Overall, 5-Chloro-2-ethoxyphenylboronic acid is a valuable compound in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C8H10BClO3
InChI:InChI=1/C8H10BClO3/c1-2-13-8-4-3-6(10)5-7(8)9(11)12/h3-5,11-12H,2H2,1H3
InChI key:InChIKey=OSMBQNBPCSSVMT-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OCC)C=CC(Cl)=C1
Synonyms:
  • (5-Chloro-2-ethoxyphenyl)boronic acid
  • 2-Ethoxy-5-chlorophenylboronic acid
  • B-(5-Chloro-2-ethoxyphenyl)boronic acid
  • Boronic acid, (5-chloro-2-ethoxyphenyl)-
  • Boronic acid, B-(5-chloro-2-ethoxyphenyl)-
  • 5-Chloro-2-ethoxyphenylboronic acid
  • 5-Chloro-2-ethoxypheylboronic acid
  • 5-Chloro-2-Ethoxyphenylboronic
  • 5-CHLORO-2-ETHOXYBENZENEBORONIC ACID
  • AKOS BRN-0696
  • See more synonyms
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