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CAS 1451393-37-5

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B-(2-Chloro-3,5-difluorophenyl)boronic acid

Description:
B-(2-Chloro-3,5-difluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated and difluorinated phenyl ring. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar organic solvents, which is common for boronic acids. 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 chlorinated and difluorinated substituents on the phenyl ring can influence the compound's reactivity and biological activity, potentially enhancing its properties for specific applications. Additionally, the compound may exhibit moderate to high stability under standard laboratory conditions, although it should be handled with care due to the presence of halogen atoms, which can impart toxicity. Overall, B-(2-Chloro-3,5-difluorophenyl)boronic acid is a versatile building block in the synthesis of complex organic molecules.
Formula:C6H4BClF2O2
InChI:InChI=1S/C6H4BClF2O2/c8-6-4(7(11)12)1-3(9)2-5(6)10/h1-2,11-12H
InChI key:InChIKey=YDJPWIRZACQGEP-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(F)=CC(F)=C1
Synonyms:
  • B-(2-Chloro-3,5-difluorophenyl)boronic acid
  • Boronic acid, B-(2-chloro-3,5-difluorophenyl)-
  • (2-Chloro-3,5-difluorophenyl)boronic acid
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