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CAS 849062-22-2

:

B-[(1E)-2-(3-Fluorophenyl)ethenyl]boronic acid

Description:
B-[(1E)-2-(3-Fluorophenyl)ethenyl]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. This compound features a vinyl group attached to a phenyl ring that has a fluorine substituent, contributing to its electronic properties and potential reactivity. The presence of the boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, which is widely used in organic synthesis for forming carbon-carbon bonds. The fluorine atom can influence the compound's lipophilicity and reactivity, making it a valuable building block in medicinal chemistry and materials science. Additionally, boronic acids are often utilized in sensor applications due to their ability to selectively bind to certain biomolecules. Overall, B-[(1E)-2-(3-Fluorophenyl)ethenyl]boronic acid is a versatile compound with significant implications in synthetic organic chemistry and potential applications in drug development.
Formula:C8H8BFO2
InChI:InChI=1S/C8H8BFO2/c10-8-3-1-2-7(6-8)4-5-9(11)12/h1-6,11-12H/b5-4+
InChI key:InChIKey=ONXKUGHKGCSZJO-SNAWJCMRSA-N
SMILES:C(=C/B(O)O)\C1=CC(F)=CC=C1
Synonyms:
  • B-[(1E)-2-(3-Fluorophenyl)ethenyl]boronic acid
  • (E)-(3-Fluorostyryl)boronic acid
  • [(E)-2-(3-Fluorophenyl)ethenyl]boronic acid
  • Boronic acid, [(1E)-2-(3-fluorophenyl)ethenyl]-
  • Boronic acid, B-[(1E)-2-(3-fluorophenyl)ethenyl]-
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