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CAS 957120-61-5

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

Description:
B-(5-Bromo-2-fluoro-3-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 applications, particularly in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a bromine atom, a fluorine atom, and a methyl group, contributing to its unique electronic and steric properties. These substitutions can influence the compound's reactivity and solubility, making it suitable for cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, the presence of the boronic acid group allows for potential applications in drug development and materials science. The compound is typically handled with care due to the reactivity of boronic acids and the presence of halogens, which may pose environmental and health risks. Overall, B-(5-Bromo-2-fluoro-3-methylphenyl)boronic acid is a valuable building block in synthetic chemistry.
Formula:C7H7BBrFO2
InChI:InChI=1S/C7H7BBrFO2/c1-4-2-5(9)3-6(7(4)10)8(11)12/h2-3,11-12H,1H3
InChI key:InChIKey=VLFDXHTXMHURJH-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(C)=CC(Br)=C1
Synonyms:
  • (5-Bromo-2-fluoro-3-methylphenyl)boronic acid
  • 5-Bromo-2-fluoro-3-methylbenzeneboronic acid
  • B-(5-Bromo-2-fluoro-3-methylphenyl)boronic acid
  • boronic acid, B-(5-bromo-2-fluoro-3-methylphenyl)-
  • 5-Bromo-2-fluoro-3-methylphenylboronic acid
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