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CAS 849052-19-3

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2-Bromo-3-Ethoxy-6-Fluorophenylboronic Acid

Description:
2-Bromo-3-Ethoxy-6-Fluorophenylboronic 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 applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a bromine atom, an ethoxy group, and a fluorine atom, contributing to its unique reactivity and solubility properties. The presence of the boronic acid moiety allows for participation in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds. Additionally, the ethoxy group enhances the compound's solubility in organic solvents, while the fluorine atom can influence the electronic properties and biological activity of the molecule. Overall, 2-Bromo-3-Ethoxy-6-Fluorophenylboronic Acid is a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, with potential applications in drug discovery and development due to its functional group diversity.
Formula:C8H9BBrFO3
InChI:InChI=1S/C8H9BBrFO3/c1-2-14-6-4-3-5(11)7(8(6)10)9(12)13/h3-4,12-13H,2H2,1H3
SMILES:CCOc1ccc(c(c1Br)B(O)O)F
Synonyms:
  • (2-Bromo-3-ethoxy-6-fluorophenyl)boronic acid
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