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CAS 1072946-16-7

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B-[4-(Methylsulfonyl)-2-(trifluoromethyl)phenyl]boronic acid

Description:
B-[4-(Methylsulfonyl)-2-(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. This compound features a phenyl ring substituted with a methylsulfonyl group and a trifluoromethyl group, contributing to its unique chemical properties. The methylsulfonyl group enhances the compound's solubility and reactivity, while the trifluoromethyl group can influence its electronic properties and lipophilicity. Typically, boronic acids are utilized in organic synthesis, particularly in Suzuki coupling reactions, which are pivotal for forming carbon-carbon bonds. The presence of the trifluoromethyl group may also impart specific biological activities or enhance the compound's interaction with biological targets. Overall, this compound is of interest in medicinal chemistry and materials science due to its functional groups and potential applications in drug development and synthesis.
Formula:C8H8BF3O4S
InChI:InChI=1S/C8H8BF3O4S/c1-17(15,16)5-2-3-7(9(13)14)6(4-5)8(10,11)12/h2-4,13-14H,1H3
InChI key:InChIKey=KRVRNINHXGLIEL-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(B(O)O)C=CC(S(C)(=O)=O)=C1
Synonyms:
  • Boronic acid, B-[4-(methylsulfonyl)-2-(trifluoromethyl)phenyl]-
  • [4-Methylsulfonyl-2-(trifluoromethyl)phenyl]boronic acid
  • B-[4-(Methylsulfonyl)-2-(trifluoromethyl)phenyl]boronic acid
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