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Atomfair 5,6-Dihydroxy-2,3-dihydro-1H-inden-1-one C9H8O3

Description 5,6-Dihydroxy-2,3-dihydro-1H-inden-1-one (CAS No. 124702-80-3) is a high-purity organic compound with the molecular formula C9H8O3. This indanone derivative features a dihydroxy-substituted aromatic ring, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. The compound is characterized by its stable crystalline structure and solubility in polar organic solvents such as methanol, ethanol, and DMSO. With an IUPAC name of 5,6-dihydroxy-2,3-dihydroinden-1-one , it is rigorously tested via HPLC, NMR, and mass spectrometry to ensure ??95% purity. Ideal for researchers exploring catechol-like reactivity, oxidative pathways, or bioactive molecule synthesis.

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Description

Description

5,6-Dihydroxy-2,3-dihydro-1H-inden-1-one (CAS No. 124702-80-3) is a high-purity organic compound with the molecular formula C9H8O3. This indanone derivative features a dihydroxy-substituted aromatic ring, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. The compound is characterized by its stable crystalline structure and solubility in polar organic solvents such as methanol, ethanol, and DMSO. With an IUPAC name of 5,6-dihydroxy-2,3-dihydroinden-1-one, it is rigorously tested via HPLC, NMR, and mass spectrometry to ensure ??95% purity. Ideal for researchers exploring catechol-like reactivity, oxidative pathways, or bioactive molecule synthesis.

  • CAS No: 124702-80-3
  • Molecular Formula: C9H8O3
  • Molecular Weight: 164.16
  • Exact Mass: 164.047344113
  • Monoisotopic Mass: 164.047344113
  • IUPAC Name: 5,6-dihydroxy-2,3-dihydroinden-1-one
  • SMILES: C1CC(=O)C2=CC(=C(C=C21)O)O
  • Synonyms: 5,6-Dihydroxy-2,3-dihydro-1H-inden-1-one, 124702-80-3, 1H-Inden-1-one, 2,3-dihydro-5,6-dihydroxy-, 5,6-DIHYDROXYINDAN-1-ONE, 2,3-dihydro-5,6-dihydroxyinden-1-one

Application

5,6-Dihydroxy-2,3-dihydro-1H-inden-1-one serves as a key precursor in the synthesis of polyphenolic compounds and neuromodulatory agents. Its catechol moiety enables applications in antioxidant studies, enzyme inhibition assays, and metal-chelating research. The compound is also investigated for potential use in neurodegenerative disease models due to its structural similarity to dopamine metabolites.

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