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CAS 66472-86-4

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(3-Aminophenyl)boronic acid hemisulfate

Description:
(3-Aminophenyl)boronic acid hemisulfate, with the CAS number 66472-86-4, is a chemical compound that features a boronic acid functional group attached to a phenyl ring that has an amino group in the meta position. This compound is typically characterized by its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in biochemical assays. The presence of the amino group enhances its solubility in polar solvents and can participate in hydrogen bonding, which may influence its reactivity and interaction with other molecules. The hemisulfate form indicates that the compound is associated with a sulfate ion, which can affect its stability and solubility in aqueous environments. Overall, (3-Aminophenyl)boronic acid hemisulfate is significant in medicinal chemistry and materials science due to its unique reactivity and functional properties.
Formula:C6H8BNO2H2O4S
InChI:InChI=1S/C6H8BNO2.H2O4S/c8-6-3-1-2-5(4-6)7(9)10;1-5(2,3)4/h1-4,9-10H,8H2;(H2,1,2,3,4)
InChI key:InChIKey=XMVGYYBQCXVVHU-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(N)=CC=C1.S(=O)(=O)(O)O
Synonyms:
  • (3-Aminophenyl)Boronic Acid Sulfate (1:1)
  • (3-Aminophenyl)boric acid hemisulfate
  • (3-Aminophenyl)boronic acid hemisulfate
  • (3-Aminophenyl)boronic acid sulfate (2:1)
  • (m-Aminophenyl)boronic acid hemisulfate
  • 3-Aminobenzeneboronic acid hemisulfate salt
  • 3-Aminophenylboric Acid Hemisulphate
  • Bis[3-dihydroxyboranyl)benzenaminium] sulfate
  • Boronic acid, (3-aminophenyl)-, sulfate (2:1)
  • Boronic acid, B-(3-aminophenyl)-, sulfate (2:1)
  • m-Aminophenylboronic acid hemisulfate
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