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CAS 536693-96-6

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Boronic acid, [2-chloro-5-(trifluoromethyl)-3-pyridinyl]-

Description:
Boronic acid, specifically 2-chloro-5-(trifluoromethyl)-3-pyridinyl boronic acid, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a pyridine ring. The compound features a chlorine atom and a trifluoromethyl group, which significantly influence its chemical reactivity and properties. The trifluoromethyl group is known for its electron-withdrawing effects, enhancing the acidity of the boronic acid group and potentially increasing the compound's reactivity in various chemical reactions, such as Suzuki coupling. The presence of the chlorine atom can also affect the compound's solubility and interaction with other molecules. Boronic acids are widely used in organic synthesis, particularly in the formation of carbon-carbon bonds and in the development of pharmaceuticals. This specific compound may exhibit unique biological activities due to its structural features, making it of interest in medicinal chemistry and material science. Overall, its characteristics make it a valuable compound in both research and industrial applications.
Formula:C6H4BClF3NO2
InChI:InChI=1S/C6H4BClF3NO2/c8-5-4(7(13)14)1-3(2-12-5)6(9,10)11/h1-2,13-14H
InChI key:InChIKey=OJUNKVOTAZHNAL-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C(C(F)(F)F)C=NC1Cl
Synonyms:
  • 2-Chloro-5-(Trifluoromethyl)Pyridine-3-Boronic Acid
  • Boronic acid, [2-chloro-5-(trifluoromethyl)-3-pyridinyl]-
  • Dihydroxy(2-chloro-5-trifluoromethyl-3-pyridyl)borane
  • boronic acid, B-[2-chloro-5-(trifluoromethyl)-3-pyridinyl]-
  • [2-Chloro-5-(trifluoromethyl)pyridin-3-yl]boronic acid
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