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CAS 850864-60-7

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B-[2-(Phenylmethoxy)-5-(trifluoromethyl)-3-pyridinyl]boronic acid

Description:
B-[2-(Phenylmethoxy)-5-(trifluoromethyl)-3-pyridinyl]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 and other nucleophiles. This compound features a pyridine ring substituted with a phenylmethoxy group and a trifluoromethyl group, contributing to its unique chemical properties. The trifluoromethyl group enhances lipophilicity and can influence the compound's reactivity and biological activity. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, which are valuable for forming carbon-carbon bonds. Additionally, this compound may exhibit potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Its structural characteristics suggest it may interact with various biological targets, making it of interest in drug discovery and development. As with many boronic acids, it is important to handle this compound with care due to its reactivity and potential environmental impact.
Formula:C13H11BF3NO3
InChI:InChI=1S/C13H11BF3NO3/c15-13(16,17)10-6-11(14(19)20)12(18-7-10)21-8-9-4-2-1-3-5-9/h1-7,19-20H,8H2
InChI key:InChIKey=OYAUWZJANZRGQV-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OCC2=CC=CC=C2)N=CC(C(F)(F)F)=C1
Synonyms:
  • Boronic acid, B-[2-(phenylmethoxy)-5-(trifluoromethyl)-3-pyridinyl]-
  • [2-[(Phenylmethyl)oxy]-5-(trifluoromethyl)-3-pyridinyl]boronic acid
  • Boronic acid, [2-(phenylmethoxy)-5-(trifluoromethyl)-3-pyridinyl]-
  • (2-(Benzyloxy)-5-(trifluoromethyl)pyridin-3-yl)boronic acid
  • B-[2-(Phenylmethoxy)-5-(trifluoromethyl)-3-pyridinyl]boronic acid
  • 2-Benzyloxy-5-(trifluoromethyl)pyridine-3-boronic acid
  • 2-(phenylmethoxy)-5-(trifluoromethyl)pyridin-3-boronic acid
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