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CAS 1256346-04-9

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B-[3-(Cyclopentyloxy)-5-(trifluoromethoxy)phenyl]boronic acid

Description:
B-[3-(Cyclopentyloxy)-5-(trifluoromethoxy)phenyl]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, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a cyclopentyloxy group and a trifluoromethoxy group, which contribute to its unique chemical properties and reactivity. The trifluoromethoxy group enhances the compound's electron-withdrawing characteristics, potentially influencing its acidity and reactivity in chemical reactions. Additionally, the cyclopentyloxy moiety may provide steric hindrance, affecting the compound's interactions with other molecules. This compound is likely to be soluble in organic solvents and may exhibit specific biological activities, making it of interest in pharmaceutical research. Its boronic acid functionality allows for participation in cross-coupling reactions, which are pivotal in the synthesis of complex organic molecules. Overall, this compound exemplifies the diverse applications of boronic acids in modern chemistry.
Formula:C12H14BF3O4
InChI:InChI=1S/C12H14BF3O4/c14-12(15,16)20-11-6-8(13(17)18)5-10(7-11)19-9-3-1-2-4-9/h5-7,9,17-18H,1-4H2
InChI key:InChIKey=HPSHUTQIASVROT-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C1=CC(B(O)O)=CC(OC2CCCC2)=C1
Synonyms:
  • B-[3-(Cyclopentyloxy)-5-(trifluoromethoxy)phenyl]boronic acid
  • Boronic acid, B-[3-(cyclopentyloxy)-5-(trifluoromethoxy)phenyl]-
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