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CAS 2121513-00-4

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B-(5-Bromo-2,3-difluoro-4-methylphenyl)boronic acid

Description:
B-(5-Bromo-2,3-difluoro-4-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. The compound features a bromine atom and two fluorine atoms on the aromatic ring, which contribute to its unique reactivity and properties. The presence of the boronic acid group allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The fluorine substituents can enhance the compound's lipophilicity and influence its biological activity, while the bromine atom can serve as a versatile handle for further functionalization. This compound is typically used in research settings, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to form stable complexes with various substrates. Its physical properties, such as solubility and melting point, can vary based on the specific conditions and solvents used. Overall, B-(5-Bromo-2,3-difluoro-4-methylphenyl)boronic acid is a significant compound in the field of synthetic organic chemistry.
Formula:C7H6BBrF2O2
InChI:InChI=1S/C7H6BBrF2O2/c1-3-5(9)2-4(8(12)13)7(11)6(3)10/h2,12-13H,1H3
InChI key:InChIKey=SRAYFRDQHIVSMN-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(F)=C(C)C(Br)=C1
Synonyms:
  • B-(5-Bromo-2,3-difluoro-4-methylphenyl)boronic acid
  • Boronic acid, B-(5-bromo-2,3-difluoro-4-methylphenyl)-
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