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CAS 958451-91-7

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[5-(trifluoromethyl)-2-thienyl]boronic acid

Description:
[5-(Trifluoromethyl)-2-thienyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a thiophene ring substituted with a trifluoromethyl group. 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 trifluoromethyl group enhances the lipophilicity and electronic properties of the molecule, making it useful in medicinal chemistry and material science. The thiophene ring contributes to the compound's aromatic character and can influence its electronic properties. Additionally, [5-(trifluoromethyl)-2-thienyl]boronic acid may exhibit solubility in organic solvents, which is advantageous for synthetic applications. Its unique structure and functional groups make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as in the development of organic electronic materials. Safety and handling precautions should be observed due to the potential reactivity of boronic acids and the toxicity associated with trifluoromethyl groups.
Formula:C5H4BF3O2S
InChI:InChI=1/C5H4BF3O2S/c7-5(8,9)3-1-2-4(12-3)6(10)11/h1-2,10-11H
SMILES:c1cc(B(O)O)sc1C(F)(F)F
Synonyms:
  • boronic acid, B-[5-(trifluoromethyl)-2-thienyl]-
  • [5-(Trifluoromethyl)-2-thienyl]boronic acid
  • 5-(trifluoromethyl)thiophen-2-ylboronic acid
  • 5-Trifluoromethyl-thiophene-2-boronic acid
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