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CAS 1072951-46-2

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B-[8-(Trifluoromethoxy)-5-quinolinyl]boronic acid

Description:
B-[8-(Trifluoromethoxy)-5-quinolinyl]boronic acid is a boronic acid derivative characterized by its unique structural features, which include a quinoline ring system and a trifluoromethoxy 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 trifluoromethoxy group enhances its lipophilicity and may influence its biological activity. Additionally, the quinoline moiety can contribute to the compound's potential as a pharmacophore in drug development. The compound is likely to be a solid at room temperature and may exhibit moderate solubility in organic solvents. Its reactivity and functionalization potential make it a valuable intermediate in the synthesis of more complex molecules. As with many boronic acids, it may also participate in Suzuki coupling reactions, which are important in the formation of carbon-carbon bonds in organic synthesis. Safety and handling precautions should be observed due to the potential reactivity of boronic acids.
Formula:C10H7BF3NO3
InChI:InChI=1S/C10H7BF3NO3/c12-10(13,14)18-8-4-3-7(11(16)17)6-2-1-5-15-9(6)8/h1-5,16-17H
InChI key:InChIKey=ZDAZERWIWJDFAV-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C=1C2=C(C(B(O)O)=CC1)C=CC=N2
Synonyms:
  • B-[8-(Trifluoromethoxy)-5-quinolinyl]boronic acid
  • Boronic acid, B-[8-(trifluoromethoxy)-5-quinolinyl]-
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