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CAS 1451392-81-6

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B-(2-Bromo-6-fluoro-3-formylphenyl)boronic acid

Description:
B-(2-Bromo-6-fluoro-3-formylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in various organic synthesis applications, particularly in Suzuki coupling reactions. This compound features a phenyl ring substituted with a bromine atom and a fluorine atom, as well as a formyl group, which contributes to its reactivity and potential applications in medicinal chemistry and material science. The presence of the boronic acid moiety allows for the formation of stable complexes with diols, making it useful in the development of sensors and in the synthesis of complex organic molecules. Additionally, the halogen substituents can influence the electronic properties of the compound, potentially enhancing its reactivity or selectivity in chemical reactions. Overall, B-(2-Bromo-6-fluoro-3-formylphenyl)boronic acid is a versatile building block in organic synthesis, with implications in drug discovery and the development of functional materials.
Formula:C7H5BBrFO3
InChI:InChI=1S/C7H5BBrFO3/c9-7-4(3-11)1-2-5(10)6(7)8(12)13/h1-3,12-13H
InChI key:InChIKey=GASAVFGFZLEBHN-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Br)C(C=O)=CC=C1F
Synonyms:
  • Boronic acid, B-(2-bromo-6-fluoro-3-formylphenyl)-
  • B-(2-Bromo-6-fluoro-3-formylphenyl)boronic acid
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