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CAS 205240-63-7

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2-Trifluoromethyl-6-chloro-5-pyridineboric acid

Description:
2-Trifluoromethyl-6-chloro-5-pyridineboric acid is an organoboron compound characterized by the presence of a pyridine ring substituted with both a trifluoromethyl group and a chlorine atom, along with a boronic acid functional group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The trifluoromethyl group contributes to the compound's lipophilicity and can influence its biological activity, while the chlorine atom may enhance its reactivity or stability. The presence of the boronic acid moiety allows for participation in Suzuki coupling reactions, which are valuable in the formation of carbon-carbon bonds. Overall, this compound is of interest in the development of pharmaceuticals and agrochemicals, as well as in materials science for creating functionalized polymers or other advanced materials. Its specific reactivity and applications would depend on the context of its use in chemical reactions or formulations.
Formula:C6H4BClF3NO2
InChI:InChI=1/C6H4BClF3NO2/c8-5-3(7(13)14)1-2-4(12-5)6(9,10)11/h1-2,13-14H
SMILES:c1cc(C(F)(F)F)nc(c1B(O)O)Cl
Synonyms:
  • [2-Chloro-6-(trifluoromethyl)-3-pyridinyl]boronic acid
  • [2-Chloro-6-(trifluoromethyl)pyridin-3-yl]boronic acid
  • Boronic acid, B-[2-chloro-6-(trifluoromethyl)-3-pyridinyl]-
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