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CAS 13494-10-5

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2′,3′-Dihydroxyacetophenone

Description:
2′,3′-Dihydroxyacetophenone, with the CAS number 13494-10-5, is an organic compound characterized by the presence of two hydroxyl (-OH) groups attached to a phenyl ring, specifically at the 2' and 3' positions relative to the acetophenone moiety. This compound typically appears as a white to off-white solid and is soluble in organic solvents, reflecting its aromatic structure. It exhibits properties such as being a potential antioxidant and has applications in various fields, including pharmaceuticals and materials science. The presence of hydroxyl groups contributes to its reactivity, allowing it to participate in hydrogen bonding and other chemical interactions. Additionally, 2′,3′-Dihydroxyacetophenone may exhibit biological activity, making it of interest in medicinal chemistry. Its synthesis can involve the hydroxylation of acetophenone or related precursors, and it can be analyzed using techniques such as NMR and mass spectrometry to confirm its structure and purity. Overall, this compound is notable for its functional groups and potential applications in diverse chemical contexts.
Formula:C8H8O3
InChI:InChI=1S/C8H8O3/c1-5(9)6-3-2-4-7(10)8(6)11/h2-4,10-11H,1H3
InChI key:InChIKey=HEJLFBLJYFSKCE-UHFFFAOYSA-N
SMILES:C(C)(=O)C1=C(O)C(O)=CC=C1
Synonyms:
  • 1-(2,3-Dihydroxyphenyl)Ethanone
  • 1-(2,3-Dihydroxyphenyl)ethan-1-one
  • 2,3-Dihydroxyacetophenone
  • 3-Acetyl-1,2-benzenediol
  • Acetophenone, 2′,3′-dihydroxy-
  • Acetophenone, dihydroxy-
  • Acetopyrocatechol
  • Ethanone, 1-(2,3-Dihydroxyphenyl)-
  • Ethanone, 1-(dihydroxyphenyl)-
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