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CAS 1162257-29-5

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B-[2-Propoxy-5-(trifluoromethyl)phenyl]boronic acid

Description:
B-[2-Propoxy-5-(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, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a trifluoromethyl group, which enhances its electronic properties and lipophilicity, and a propoxy group that contributes to its solubility in organic solvents. The trifluoromethyl group is notable for imparting unique reactivity and stability, while the propoxy group can influence the compound's interaction with biological systems. This boronic acid derivative is of interest in medicinal chemistry and materials science, particularly for its potential applications in drug development and organic synthesis. Its properties, such as solubility, stability, and reactivity, can vary based on environmental conditions and the presence of other functional groups in a reaction mixture.
Formula:C10H12BF3O3
InChI:InChI=1S/C10H12BF3O3/c1-2-5-17-9-4-3-7(10(12,13)14)6-8(9)11(15)16/h3-4,6,15-16H,2,5H2,1H3
InChI key:InChIKey=PVXWTWSMVNMSTE-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OCCC)C=CC(C(F)(F)F)=C1
Synonyms:
  • B-[2-Propoxy-5-(trifluoromethyl)phenyl]boronic acid
  • 2-Propoxy-5-(trifluoromethyl)phenylboronic acid
  • Boronic acid, B-[2-propoxy-5-(trifluoromethyl)phenyl]-
  • [2-Propoxy-5-(trifluoromethyl)phenyl]boronic acid
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