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CAS 1190095-08-9

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B-[2-Fluoro-5-[[(4-methylphenyl)amino]methyl]phenyl]boronic acid

Description:
B-[2-Fluoro-5-[[(4-methylphenyl)amino]methyl]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 medicinal chemistry and materials science. The compound features a fluorinated phenyl ring, which can influence its electronic properties and reactivity. The presence of the 4-methylphenyl group suggests potential hydrophobic interactions, which may enhance its biological activity or solubility in organic solvents. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the specific structural features of this compound may contribute to its potential as a pharmaceutical agent, particularly in targeting specific biological pathways or as a probe in chemical biology. Overall, the unique combination of functional groups and structural characteristics makes this compound of interest in both research and industrial applications.
Formula:C14H15BFNO2
InChI:InChI=1S/C14H15BFNO2/c1-10-2-5-12(6-3-10)17-9-11-4-7-14(16)13(8-11)15(18)19/h2-8,17-19H,9H2,1H3
InChI key:InChIKey=CEVNDBLSQXIRNX-UHFFFAOYSA-N
SMILES:C(NC1=CC=C(C)C=C1)C2=CC(B(O)O)=C(F)C=C2
Synonyms:
  • Boronic acid, B-[2-fluoro-5-[[(4-methylphenyl)amino]methyl]phenyl]-
  • B-[2-Fluoro-5-[[(4-methylphenyl)amino]methyl]phenyl]boronic acid
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