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CAS 352525-82-7

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5-Bromo-2-ethoxyphenylboronic acid

Description:
5-Bromo-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. This compound features a bromine atom and an ethoxy group attached to a phenyl ring, contributing to its unique reactivity and solubility properties. Typically, boronic acids are utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds. The presence of the bromine substituent enhances its electrophilic character, making it a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals. Additionally, the ethoxy group can influence the compound's solubility in organic solvents, facilitating its use in diverse chemical reactions. Overall, 5-Bromo-2-ethoxyphenylboronic acid is a versatile reagent in synthetic organic chemistry, with applications extending to materials science and medicinal chemistry.
Formula:C8H10BBrO3
InChI:InChI=1S/C8H10BBrO3/c1-2-13-8-4-3-6(10)5-7(8)9(11)12/h3-5,11-12H,2H2,1H3
InChI key:InChIKey=PMWQJPWDAQROND-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OCC)C=CC(Br)=C1
Synonyms:
  • Boronic acid, (5-bromo-2-ethoxyphenyl)-
  • Boronic acid, B-(5-bromo-2-ethoxyphenyl)-
  • 5-Bromo-2-ethoxyphenylboronic acid
  • B-(5-Bromo-2-ethoxyphenyl)boronic acid
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