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CAS 871332-97-7

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[3-methoxy-5-(trifluoromethyl)phenyl]boronic acid

Description:
[3-Methoxy-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 and other nucleophiles. This compound features a phenyl ring substituted with a methoxy group and a trifluoromethyl group, which can influence its electronic properties and reactivity. The methoxy group typically enhances solubility in organic solvents and may participate in hydrogen bonding, while the trifluoromethyl group can impart unique electronic characteristics, making the compound potentially useful in medicinal chemistry and materials science. The boronic acid moiety allows for applications in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the compound's structure suggests potential interactions with biological targets, making it of interest in drug development. Overall, [3-methoxy-5-(trifluoromethyl)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C8H8BF3O3
InChI:InChI=1/C8H8BF3O3/c1-15-7-3-5(8(10,11)12)2-6(4-7)9(13)14/h2-4,13-14H,1H3
SMILES:COc1cc(cc(c1)B(O)O)C(F)(F)F
Synonyms:
  • boronic acid, B-[3-methoxy-5-(trifluoromethyl)phenyl]-
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