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CAS 1218790-76-1

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Boronic acid, B-(5-amino-2,4-difluorophenyl)-, hydrochloride (1:1)

Description:
Boronic acid, B-(5-amino-2,4-difluorophenyl)-, hydrochloride (1:1) is a chemical compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. The compound features a 5-amino group and two fluorine atoms at the 2 and 4 positions of the phenyl ring, which contribute to its unique reactivity and potential applications in medicinal chemistry and materials science. The hydrochloride form indicates that the compound is a salt formed with hydrochloric acid, enhancing its solubility in polar solvents. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis, particularly in the development of boronate esters and in Suzuki coupling reactions. The presence of amino and fluorine substituents may influence the compound's biological activity and interaction with various biological targets. Overall, this compound's structure suggests potential utility in drug development and as a building block in organic synthesis.
Formula:C6H6BF2NO2·ClH
InChI:InChI=1S/C6H6BF2NO2.ClH/c8-4-2-5(9)6(10)1-3(4)7(11)12;/h1-2,11-12H,10H2;1H
InChI key:InChIKey=HAKZXGNYHOUDRS-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C=C(F)C(N)=C1.Cl
Synonyms:
  • Boronic acid, B-(5-amino-2,4-difluorophenyl)-, hydrochloride (1:1)
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