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CAS 62932-92-7

:

2-Bromo-1-(3,5-dihydroxyphenyl)ethanone

Description:
2-Bromo-1-(3,5-dihydroxyphenyl)ethanone, with the CAS number 62932-92-7, is an organic compound characterized by its bromine substitution and the presence of a ketone functional group. This compound features a phenolic structure with two hydroxyl groups located at the 3 and 5 positions on the aromatic ring, contributing to its potential reactivity and biological activity. The bromine atom enhances the compound's electrophilic character, making it useful in various synthetic applications, including medicinal chemistry. The presence of the ethanone moiety indicates that it has a carbonyl group adjacent to the ethyl group, which can participate in nucleophilic addition reactions. This compound may exhibit interesting properties such as antioxidant activity due to the hydroxyl groups, and it could serve as a precursor for further chemical modifications. Its solubility and stability in different solvents can vary, influencing its application in research and industry. Overall, 2-Bromo-1-(3,5-dihydroxyphenyl)ethanone is a versatile compound with potential implications in pharmacology and organic synthesis.
Formula:C8H7BrO3
InChI:InChI=1/C8H7BrO3/c9-4-8(12)5-1-6(10)3-7(11)2-5/h1-3,10-11H,4H2
InChI key:InChIKey=WUXKAYZEXYAYIT-UHFFFAOYSA-N
SMILES:C(CBr)(=O)C1=CC(O)=CC(O)=C1
Synonyms:
  • 2-Bromo-1-(3,5-dihydroxyphenyl)ethan-1-one
  • Ethanone, 2-Bromo-1-(3,5-Dihydroxyphenyl)-
  • 2-Bromo-1-(3,5-dihydroxyphenyl)ethanone
  • 2-BROMO-1-(3,5-DIHYDROXYPHENYL)ETHANONE
  • 2-Bromo-1-(3′,5′-dihydroxyphenyl)ethanone
  • 3,5-DIHYDROXY-ALPHA-BROMOACETOPHENONE
  • 3,5-DIHYDROXY-ALFA-BROMOACETOPHENONE
  • 3',5'-Dihydroxyphenacyl bromide
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