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CAS 957063-10-4

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[4-(2-aminophenoxy)phenyl]boronic acid hydrochloride

Description:
[4-(2-Aminophenoxy)phenyl]boronic acid hydrochloride is a boronic acid derivative characterized by its boron-containing 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. This compound features an amino group and a phenoxy group, contributing to its potential biological activity and solubility properties. The hydrochloride form indicates that it is a salt, which typically enhances its stability and solubility in aqueous solutions. The presence of the boronic acid moiety allows for participation in Suzuki coupling reactions, a key method in the formation of carbon-carbon bonds in organic synthesis. Additionally, the compound may exhibit properties relevant to drug development, particularly in targeting specific biological pathways. Its molecular structure and functional groups suggest potential applications in pharmaceuticals, particularly in the development of compounds that interact with biological targets through reversible binding mechanisms. Overall, [4-(2-aminophenoxy)phenyl]boronic acid hydrochloride is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C12H13BClNO3
InChI:InChI=1/C12H12BNO3.ClH/c14-11-3-1-2-4-12(11)17-10-7-5-9(6-8-10)13(15)16;/h1-8,15-16H,14H2;1H
SMILES:c1ccc(c(c1)N)Oc1ccc(cc1)B(O)O.Cl
Synonyms:
  • 4-(2-Aminophenoxy)phenylboronic acid, HCl
  • 4-(2-Aminophenoxy)benzeneboronic acid hydrochloride
  • (4-(2-AMinophenoxy)phenyl)boronic acid hydrochloride
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