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CAS 1256345-99-9

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

Description:
B-[2-(2-Methylpropoxy)-5-(trifluoromethyl)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. This compound features a phenyl ring substituted with a trifluoromethyl group, enhancing its lipophilicity and potentially influencing its reactivity and solubility in organic solvents. The presence of a 2-methylpropoxy group contributes to its steric bulk, which can affect its interactions in chemical reactions, particularly in cross-coupling reactions commonly utilized in organic synthesis. Boronic acids are often used in medicinal chemistry and materials science due to their ability to participate in Suzuki-Miyaura coupling reactions, making them valuable in the synthesis of complex organic molecules. Additionally, the trifluoromethyl group can impart unique electronic properties, making this compound of interest in the development of pharmaceuticals and agrochemicals. Overall, this compound's structure suggests potential applications in various fields, including organic synthesis and drug development.
Formula:C11H14BF3O3
InChI:InChI=1S/C11H14BF3O3/c1-7(2)6-18-10-4-3-8(11(13,14)15)5-9(10)12(16)17/h3-5,7,16-17H,6H2,1-2H3
InChI key:InChIKey=YYWZYPLOMFBKDT-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OCC(C)C)C=CC(C(F)(F)F)=C1
Synonyms:
  • Boronic acid, B-[2-(2-methylpropoxy)-5-(trifluoromethyl)phenyl]-
  • B-[2-(2-Methylpropoxy)-5-(trifluoromethyl)phenyl]boronic acid
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