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CAS 85006-23-1

:

3-Aminophenylboronic acid hydrochloride

Description:
3-Aminophenylboronic acid hydrochloride is an organic compound characterized by the presence of both an amine and a boronic acid functional group. It typically appears as a white to off-white crystalline solid and is soluble in water and polar organic solvents, which enhances its utility in various chemical reactions. The compound features a boron atom bonded to a phenyl ring that is substituted with an amino group, making it a valuable reagent in organic synthesis, particularly in Suzuki coupling reactions for the formation of carbon-carbon bonds. Its hydrochloride form indicates the presence of a hydrochloric acid moiety, which can influence its solubility and reactivity. Additionally, 3-aminophenylboronic acid hydrochloride is often used in medicinal chemistry and materials science due to its ability to form reversible covalent bonds with diols, making it useful in the development of sensors and drug delivery systems. Safety precautions should be taken when handling this compound, as with many boron-containing chemicals, due to potential irritant properties.
Formula:C6H8BNO2·ClH
InChI:InChI=1S/C6H8BNO2.ClH/c8-6-3-1-2-5(4-6)7(9)10;/h1-4,9-10H,8H2;1H
InChI key:InChIKey=QBMHZZHJIBUPOX-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(N)=CC=C1.Cl
Synonyms:
  • (m-Aminophenyl)boronic acid hydrochloride
  • (m-Aminophenyl)metaboric acid HCl
  • (m-Aminophenyl)metaboric acid hydrochloride
  • 3-Aminophenylboronic Acid Hydrochloride
  • 3-Aminophenylboronicacid hydrochloride
  • Boronic acid, (3-aminophenyl)-, hydrochloride
  • Boronic acid, B-(3-aminophenyl)-, hydrochloride (1:1)
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