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CAS 2121513-70-8

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B-[2-Chloro-5-fluoro-3-(trifluoromethyl)phenyl]boronic acid

Description:
B-[2-Chloro-5-fluoro-3-(trifluoromethyl)phenyl]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 other nucleophiles. This compound features a phenyl ring substituted with a chlorine atom, a fluorine atom, and a trifluoromethyl group, contributing to its unique electronic properties and potential reactivity. The presence of these halogen substituents can influence the compound's lipophilicity, stability, and interaction with biological targets. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, which are valuable for forming carbon-carbon bonds. Additionally, the trifluoromethyl group can enhance the compound's biological activity and selectivity in medicinal chemistry applications. Overall, B-[2-Chloro-5-fluoro-3-(trifluoromethyl)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C7H4BClF4O2
InChI:InChI=1S/C7H4BClF4O2/c9-6-4(7(11,12)13)1-3(10)2-5(6)8(14)15/h1-2,14-15H
InChI key:InChIKey=YBPUHOKTPNETHW-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(Cl)C(B(O)O)=CC(F)=C1
Synonyms:
  • Boronic acid, B-[2-chloro-5-fluoro-3-(trifluoromethyl)phenyl]-
  • B-[2-Chloro-5-fluoro-3-(trifluoromethyl)phenyl]boronic acid
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