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CAS 947533-15-5

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B-[4-[(Trifluoromethyl)thio]phenyl]boronic acid

Description:
B-[4-[(Trifluoromethyl)thio]phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has a trifluoromethylthio substituent. This compound typically exhibits properties such as high reactivity due to the boronic acid moiety, which can participate in various chemical reactions, including Suzuki coupling and other cross-coupling reactions. The trifluoromethylthio group enhances the compound's lipophilicity and may influence its electronic properties, making it useful in medicinal chemistry and materials science. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications. The presence of fluorine atoms often imparts unique characteristics, such as increased stability and altered solubility in organic solvents. Overall, B-[4-[(Trifluoromethyl)thio]phenyl]boronic acid is a versatile compound with potential applications in organic synthesis and pharmaceutical development.
Formula:C7H6BF3O2S
InChI:InChI=1S/C7H6BF3O2S/c9-7(10,11)14-6-3-1-5(2-4-6)8(12)13/h1-4,12-13H
InChI key:InChIKey=LCTCJAHRVYNYTQ-UHFFFAOYSA-N
SMILES:S(C(F)(F)F)C1=CC=C(B(O)O)C=C1
Synonyms:
  • (4-Trifluoromethylsulfanylphenyl)boronic acid
  • 4-(Trifluoromethylthio)-Benzeneboronic Acid
  • 4-(Trifluoromethylthio)phenylboronic acid
  • B-[4-[(Trifluoromethyl)thio]phenyl]boronic acid
  • Boronic acid, B-[4-[(trifluoromethyl)thio]phenyl]-
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