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CAS 870718-00-6

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B-(3-Bromo-2-ethoxy-5-methylphenyl)boronic acid

Description:
B-(3-Bromo-2-ethoxy-5-methylphenyl)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 organic synthesis applications, particularly in Suzuki coupling reactions. The compound features a bromine atom and an ethoxy group attached to a phenyl ring, contributing to its reactivity and solubility properties. The presence of the methyl group on the aromatic ring can influence the electronic properties and steric hindrance, affecting its reactivity in chemical reactions. This compound is typically used in medicinal chemistry and materials science for the development of pharmaceuticals and advanced materials. Its boronic acid functionality allows for the formation of stable complexes with biomolecules, making it a valuable tool in biochemical research. Safety data should be consulted before handling, as boronic acids can pose health risks if not managed properly.
Formula:C9H12BBrO3
InChI:InChI=1S/C9H12BBrO3/c1-3-14-9-7(10(12)13)4-6(2)5-8(9)11/h4-5,12-13H,3H2,1-2H3
InChI key:InChIKey=BTBLZNZUELXCOT-UHFFFAOYSA-N
SMILES:O(CC)C1=C(B(O)O)C=C(C)C=C1Br
Synonyms:
  • Boronic acid, B-(3-bromo-2-ethoxy-5-methylphenyl)-
  • (3-Bromo-2-ethoxy-5-methylphenyl)boronic acid
  • 3-Bromo-2-ethoxy-5-methylphenylboronic acid
  • Boronic acid, (3-bromo-2-ethoxy-5-methylphenyl)-
  • B-(3-Bromo-2-ethoxy-5-methylphenyl)boronic acid
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