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Atomfair 2-(6,7-dimethoxy-1H-indol-3-yl)ethanol C12H15NO3

Description 2-(6,7-dimethoxy-1H-indol-3-yl)ethanol (CAS No. 153718-67-3) is a high-purity indole derivative with the molecular formula C12H15NO3. This compound features a 6,7-dimethoxy-substituted indole core linked to an ethanol moiety, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 221.25 g/mol, it is supplied as a fine powder or crystalline solid, characterized by rigorous QC standards including HPLC, NMR, and MS to ensure ??95% purity. Ideal for researchers exploring indole-based bioactive molecules, this compound is packaged under inert conditions to guarantee stability and longevity. Store in a cool, dry place away from light and moisture for…

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Description

Description

2-(6,7-dimethoxy-1H-indol-3-yl)ethanol (CAS No. 153718-67-3) is a high-purity indole derivative with the molecular formula C12H15NO3. This compound features a 6,7-dimethoxy-substituted indole core linked to an ethanol moiety, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 221.25 g/mol, it is supplied as a fine powder or crystalline solid, characterized by rigorous QC standards including HPLC, NMR, and MS to ensure ??95% purity. Ideal for researchers exploring indole-based bioactive molecules, this compound is packaged under inert conditions to guarantee stability and longevity. Store in a cool, dry place away from light and moisture for optimal shelf life.

  • CAS No: 153718-67-3
  • Molecular Formula: C12H15NO3
  • Molecular Weight: 221.25
  • Exact Mass: 221.10519334
  • Monoisotopic Mass: 221.10519334
  • IUPAC Name: 2-(6,7-dimethoxy-1H-indol-3-yl)ethanol
  • SMILES: COC1=C(C2=C(C=C1)C(=CN2)CCO)OC
  • Synonyms: 153718-67-3, 2-(6,7-dimethoxy-1H-indol-3-yl)ethanol, 2-(6,7-Dimethoxy-1H-indol-3-yl)ethan-1-ol

Application

2-(6,7-dimethoxy-1H-indol-3-yl)ethanol is a versatile building block in medicinal chemistry, particularly for synthesizing analogs of biologically active indole alkaloids. It serves as a precursor in the development of serotonin receptor modulators and kinase inhibitors. Researchers also utilize this compound in the study of plant growth regulators due to its structural similarity to auxin-related metabolites. Its dimethoxy groups enhance solubility for in vitro assays.

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