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Atomfair 2-hydroxy-3-(1H-indol-3-yl)butanoic acid C12H13NO3

Description 2-Hydroxy-3-(1H-indol-3-yl)butanoic acid (CAS No. 259209-22-8) is a high-purity indole derivative with the molecular formula C12H13NO3. This specialized compound features a hydroxyl group and a carboxylic acid moiety on a butanoic acid backbone, coupled with an indole ring, making it a valuable intermediate for organic synthesis and pharmaceutical research. With a molecular weight of 219.24 g/mol, it is supplied as a fine powder or crystalline solid, ensuring optimal solubility and reactivity for advanced applications. Ideal for researchers in medicinal chemistry, this product is rigorously tested for purity (??95% by HPLC) and stability, meeting the stringent requirements of laboratory and industrial…

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Description

Description

2-Hydroxy-3-(1H-indol-3-yl)butanoic acid (CAS No. 259209-22-8) is a high-purity indole derivative with the molecular formula C12H13NO3. This specialized compound features a hydroxyl group and a carboxylic acid moiety on a butanoic acid backbone, coupled with an indole ring, making it a valuable intermediate for organic synthesis and pharmaceutical research. With a molecular weight of 219.24 g/mol, it is supplied as a fine powder or crystalline solid, ensuring optimal solubility and reactivity for advanced applications. Ideal for researchers in medicinal chemistry, this product is rigorously tested for purity (??95% by HPLC) and stability, meeting the stringent requirements of laboratory and industrial use. Store in a cool, dry place under inert conditions to maintain integrity.

  • CAS No: 259209-22-8
  • Molecular Formula: C12H13NO3
  • Molecular Weight: 219.24
  • Exact Mass: 219.08954328
  • Monoisotopic Mass: 219.08954328
  • IUPAC Name: 2-hydroxy-3-(1H-indol-3-yl)butanoic acid
  • SMILES: CC(C1=CNC2=CC=CC=C21)C(C(=O)O)O
  • Synonyms: 2-hydroxy-3-(1H-indol-3-yl)butanoic acid, 21193-78-2, SCHEMBL7817298, CHEBI:182075, NUFXPJOTSOMKFZ-UHFFFAOYSA-N

Application

2-Hydroxy-3-(1H-indol-3-yl)butanoic acid serves as a key building block in the synthesis of bioactive indole alkaloids and pharmaceutical intermediates. Its unique structure enables applications in the development of serotonin analogs and enzyme inhibitors for neurological research. Researchers also utilize this compound in peptidomimetics and as a chiral auxiliary in asymmetric synthesis.

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