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CAS 850568-45-5

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Boronic acid, (3-amino-4-chlorophenyl)-, hydrochloride

Description:
Boronic acid, (3-amino-4-chlorophenyl)-, hydrochloride, with the CAS number 850568-45-5, is a chemical compound characterized by the presence of a boronic acid functional group attached to a chlorinated aromatic ring that also contains an amino group. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, which is a common trait for many boronic acids. The presence of the amino group contributes to its potential as a ligand in various chemical reactions, particularly in Suzuki coupling reactions, which are important in organic synthesis for forming carbon-carbon bonds. The hydrochloride form indicates that the compound is a salt, which can enhance its stability and solubility. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in biochemical applications, including drug development and sensor technology. Overall, this compound's unique structure and functional groups make it a valuable entity in both synthetic and medicinal chemistry.
Formula:C6H7BClNO2·ClH
InChI:InChI=1S/C6H7BClNO2.ClH/c8-5-2-1-4(7(10)11)3-6(5)9;/h1-3,10-11H,9H2;1H
InChI key:InChIKey=MTMLYYSBEQYCDJ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(N)=C(Cl)C=C1.Cl
Synonyms:
  • (3-Amino-4-chlorophenyl)boronic acid hydrochloride (1:1)
  • Boronic acid, (3-amino-4-chlorophenyl)-, hydrochloride
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