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CAS 957035-32-4

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4-Bromo-2-fluoro-6-methoxyphenylboronic acid

Description:
4-Bromo-2-fluoro-6-methoxyphenylboronic 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. This compound features a phenyl ring substituted with a bromine atom, a fluorine atom, and a methoxy group, contributing to its unique electronic and steric properties. The presence of the boronic acid group allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, the methoxy group can influence the compound's solubility and reactivity. The compound's molecular structure and substituents can affect its physical properties, such as melting point and solubility in various solvents. Overall, 4-Bromo-2-fluoro-6-methoxyphenylboronic acid is a valuable building block in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C7H7BBrFO3
InChI:InChI=1/C7H7BBrFO3/c1-13-6-3-4(9)2-5(10)7(6)8(11)12/h2-3,11-12H,1H3
SMILES:COc1cc(cc(c1B(O)O)F)Br
Synonyms:
  • (4-Bromo-2-fluoro-6-methoxyphenyl)boronic acid
  • boronic acid, B-(4-bromo-2-fluoro-6-methoxyphenyl)-
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