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CAS 1072952-21-6

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B-[2-(1-Methylethoxy)-4-(trifluoromethyl)phenyl]boronic acid

Description:
B-[2-(1-Methylethoxy)-4-(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, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a trifluoromethyl group, which enhances its electronic properties and lipophilicity, potentially influencing its reactivity and solubility in organic solvents. The presence of the 1-methylethoxy group contributes to its steric bulk, which can affect its interaction with biological targets or catalysts. This compound may be utilized in cross-coupling reactions, particularly in the formation of carbon-carbon bonds, and could serve as a building block in the synthesis of more complex molecules. Additionally, the trifluoromethyl group is often associated with increased metabolic stability and bioactivity in pharmaceutical applications. Overall, B-[2-(1-Methylethoxy)-4-(trifluoromethyl)phenyl]boronic acid exhibits unique properties that make it a valuable compound in both research and industrial contexts.
Formula:C10H12BF3O3
InChI:InChI=1S/C10H12BF3O3/c1-6(2)17-9-5-7(10(12,13)14)3-4-8(9)11(15)16/h3-6,15-16H,1-2H3
InChI key:InChIKey=IGJULKZGKYXWAR-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=C(B(O)O)C=CC(C(F)(F)F)=C1
Synonyms:
  • B-[2-(1-Methylethoxy)-4-(trifluoromethyl)phenyl]boronic acid
  • Boronic acid, B-[2-(1-methylethoxy)-4-(trifluoromethyl)phenyl]-
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