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CAS 2096339-76-1

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B-[6-Chloro-2-(trifluoromethyl)-3-pyridinyl]boronic acid

Description:
B-[6-Chloro-2-(trifluoromethyl)-3-pyridinyl]boronic acid is a boronic acid derivative characterized by its unique structural features, including a pyridine ring substituted with a chlorine atom and a trifluoromethyl 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 presence of the trifluoromethyl group enhances its lipophilicity and may influence its biological activity. Additionally, the chlorine substituent can affect the electronic properties of the molecule, potentially impacting its reactivity and interactions with biological targets. As a boronic acid, it may also participate in Suzuki coupling reactions, which are valuable in the formation of carbon-carbon bonds in organic synthesis. Overall, this compound's unique functional groups and reactivity profile make it a subject of interest in both research and industrial applications.
Formula:C6H4BClF3NO2
InChI:InChI=1S/C6H4BClF3NO2/c8-4-2-1-3(7(13)14)5(12-4)6(9,10)11/h1-2,13-14H
InChI key:InChIKey=OLRXJTUODFYILY-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(B(O)O)C=CC(Cl)=N1
Synonyms:
  • B-[6-Chloro-2-(trifluoromethyl)-3-pyridinyl]boronic acid
  • Boronic acid, B-[6-chloro-2-(trifluoromethyl)-3-pyridinyl]-
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