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CAS 1451393-06-8

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B-(4-Bromo-2-fluoro-3-formylphenyl)boronic acid

Description:
B-(4-Bromo-2-fluoro-3-formylphenyl)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 and is widely used in organic synthesis and medicinal chemistry. The 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 cross-coupling reactions, such as Suzuki-Miyaura coupling. The presence of the boronic acid moiety allows for the formation of stable complexes with various substrates, making it valuable in the development of pharmaceuticals and agrochemicals. Additionally, the specific halogen substitutions can influence the electronic properties and steric hindrance of the molecule, affecting its reactivity and interaction with biological targets. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their role in the development of complex organic molecules.
Formula:C7H5BBrFO3
InChI:InChI=1S/C7H5BBrFO3/c9-6-2-1-5(8(12)13)7(10)4(6)3-11/h1-3,12-13H
InChI key:InChIKey=UIXKWZUGARWZOM-UHFFFAOYSA-N
SMILES:C(=O)C1=C(F)C(B(O)O)=CC=C1Br
Synonyms:
  • B-(4-Bromo-2-fluoro-3-formylphenyl)boronic acid
  • Boronic acid, B-(4-bromo-2-fluoro-3-formylphenyl)-
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