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CAS 2096341-62-5

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B-[3-Ethoxy-4-fluoro-5-(trifluoromethyl)phenyl]boronic acid

Description:
B-[3-Ethoxy-4-fluoro-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, making it useful in various applications, particularly in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with an ethoxy group, a fluorine atom, and a trifluoromethyl group, contributing to its unique electronic and steric properties. The presence of the trifluoromethyl group enhances lipophilicity and can influence the compound's reactivity and biological activity. Boronic acids are often utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the specific substitutions on the phenyl ring can affect the compound's solubility, stability, and interaction with biological targets. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their potential in drug development.
Formula:C9H9BF4O3
InChI:InChI=1S/C9H9BF4O3/c1-2-17-7-4-5(10(15)16)3-6(8(7)11)9(12,13)14/h3-4,15-16H,2H2,1H3
InChI key:InChIKey=IMPXHVASTNGBSE-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(F)C(OCC)=CC(B(O)O)=C1
Synonyms:
  • Boronic acid, B-[3-ethoxy-4-fluoro-5-(trifluoromethyl)phenyl]-
  • B-[3-Ethoxy-4-fluoro-5-(trifluoromethyl)phenyl]boronic acid
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