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CAS 2121512-48-7

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B-[2-Bromo-6-fluoro-3-(methylthio)phenyl]boronic acid

Description:
B-[2-Bromo-6-fluoro-3-(methylthio)phenyl]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, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a bromine atom, a fluorine atom, and a methylthio group, which contribute to its unique reactivity and potential biological activity. The presence of these substituents can influence the compound's electronic properties, solubility, and interaction with biological targets. Boronic acids are often utilized in Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules. Additionally, the specific arrangement of substituents in this compound may affect its stability and reactivity under various conditions, making it a subject of interest in both academic research and industrial applications.
Formula:C7H7BBrFO2S
InChI:InChI=1S/C7H7BBrFO2S/c1-13-5-3-2-4(10)6(7(5)9)8(11)12/h2-3,11-12H,1H3
InChI key:InChIKey=XDMGUNOXCGJUEO-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Br)C(SC)=CC=C1F
Synonyms:
  • Boronic acid, B-[2-bromo-6-fluoro-3-(methylthio)phenyl]-
  • B-[2-Bromo-6-fluoro-3-(methylthio)phenyl]boronic acid
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