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CAS 1072951-75-7

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B-[2-Bromo-6-fluoro-3-(1-methylethoxy)phenyl]boronic acid

Description:
B-[2-Bromo-6-fluoro-3-(1-methylethoxy)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 and a fluorine atom, which can influence its reactivity and biological activity. The presence of the 1-methylethoxy group enhances its solubility and stability in organic solvents. Boronic acids are typically used in Suzuki coupling reactions, a key method for forming carbon-carbon bonds, and this specific compound may serve as a valuable intermediate in the synthesis of more complex molecules. Additionally, the unique combination of halogen substituents may impart specific electronic properties, affecting the compound's reactivity and potential applications in drug development or materials science. As with many organoboron compounds, careful handling and storage are recommended due to their sensitivity to moisture and air.
Formula:C9H11BBrFO3
InChI:InChI=1S/C9H11BBrFO3/c1-5(2)15-7-4-3-6(12)8(9(7)11)10(13)14/h3-5,13-14H,1-2H3
InChI key:InChIKey=UVXVGFZUDLIHKI-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Br)C(OC(C)C)=CC=C1F
Synonyms:
  • B-[2-Bromo-6-fluoro-3-(1-methylethoxy)phenyl]boronic acid
  • Boronic acid, B-[2-bromo-6-fluoro-3-(1-methylethoxy)phenyl]-
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