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CAS 1256346-03-8

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B-[3-(2-Methylpropoxy)-5-(trifluoromethoxy)phenyl]boronic acid

Description:
B-[3-(2-Methylpropoxy)-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 2-methylpropoxy group and a trifluoromethoxy group, which contribute to its unique chemical properties, such as increased lipophilicity and potential for enhanced reactivity. The trifluoromethoxy group can influence the electronic properties of the molecule, potentially enhancing its ability to participate in reactions like Suzuki coupling. Additionally, boronic acids are often utilized in the development of pharmaceuticals and agrochemicals due to their ability to act as intermediates in the synthesis of complex organic molecules. The compound's solubility, stability, and reactivity can be influenced by the presence of these substituents, making it a subject of interest in both research and industrial applications.
Formula:C11H14BF3O4
InChI:InChI=1S/C11H14BF3O4/c1-7(2)6-18-9-3-8(12(16)17)4-10(5-9)19-11(13,14)15/h3-5,7,16-17H,6H2,1-2H3
InChI key:InChIKey=CJDCUTJVSGONQM-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C1=CC(OCC(C)C)=CC(B(O)O)=C1
Synonyms:
  • B-[3-(2-Methylpropoxy)-5-(trifluoromethoxy)phenyl]boronic acid
  • Boronic acid, B-[3-(2-methylpropoxy)-5-(trifluoromethoxy)phenyl]-
  • 3-Isobutoxy-5-(trifluoromethoxy)phenylboronic acid
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