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CAS 523-88-6

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1,2-Bis(5-bromo-2-hydroxyphenyl)-1,2-ethanedione

Description:
1,2-Bis(5-bromo-2-hydroxyphenyl)-1,2-ethanedione, commonly referred to by its CAS number 523-88-6, is an organic compound characterized by its structure, which features two 5-bromo-2-hydroxyphenyl groups attached to a central ethanedione moiety. This compound exhibits notable properties due to the presence of bromine and hydroxyl functional groups, which can influence its reactivity and solubility. It is typically a solid at room temperature and may exhibit a range of colors depending on its purity and crystalline form. The bromine substituents enhance its electrophilic character, making it useful in various chemical reactions, including those involving nucleophilic attack. Additionally, the hydroxyl groups can participate in hydrogen bonding, affecting its solubility in polar solvents. This compound may find applications in organic synthesis, materials science, and potentially in biological systems, although specific applications would depend on further research into its properties and behavior in different environments. Safety data should be consulted due to the presence of bromine, which can pose health risks.
Formula:C14H8Br2O4
InChI:InChI=1S/C14H8Br2O4/c15-7-1-3-11(17)9(5-7)13(19)14(20)10-6-8(16)2-4-12(10)18/h1-6,17-18H
InChI key:InChIKey=AAOYLOCWJSLLJU-UHFFFAOYSA-N
SMILES:C(C(=O)C1=C(O)C=CC(Br)=C1)(=O)C2=C(O)C=CC(Br)=C2
Synonyms:
  • Salicil, 5,5′-dibromo-
  • DBS
  • 1,2-Ethanedione, 1,2-bis(5-bromo-2-hydroxyphenyl)-
  • 1,2-Bis(5-bromo-2-hydroxyphenyl)-1,2-ethanedione
  • Ethanedione, bis(5-bromo-2-hydroxyphenyl)-
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