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Atomfair 1-Amino-2-hydroxyindane C9H11NO

Description 1-Amino-2-hydroxyindane (CAS No. 136030-00-7) is a high-purity organic compound with the molecular formula C9H11NO and IUPAC name 1-amino-2,3-dihydro-1H-inden-2-ol . This chiral building block is widely utilized in pharmaceutical research, asymmetric synthesis, and fine chemical applications. The compound features both amino and hydroxyl functional groups on a fused bicyclic indane scaffold, making it a versatile intermediate for medicinal chemistry and catalyst design. Available as a white to off-white crystalline powder, our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied with comprehensive analytical data including1H NMR,13C NMR, and mass spectrometry reports. Suitable for use in drug discovery…

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Description

Description

1-Amino-2-hydroxyindane (CAS No. 136030-00-7) is a high-purity organic compound with the molecular formula C9H11NO and IUPAC name 1-amino-2,3-dihydro-1H-inden-2-ol. This chiral building block is widely utilized in pharmaceutical research, asymmetric synthesis, and fine chemical applications. The compound features both amino and hydroxyl functional groups on a fused bicyclic indane scaffold, making it a versatile intermediate for medicinal chemistry and catalyst design. Available as a white to off-white crystalline powder, our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied with comprehensive analytical data including 1H NMR, 13C NMR, and mass spectrometry reports. Suitable for use in drug discovery programs and as a precursor for novel chiral ligands.

  • CAS No: 136030-00-7
  • Molecular Formula: C9H11NO
  • Molecular Weight: 149.19
  • Exact Mass: 149.084063974
  • Monoisotopic Mass: 149.084063974
  • IUPAC Name: 1-amino-2,3-dihydro-1H-inden-2-ol
  • SMILES: C1C(C(C2=CC=CC=C21)N)O
  • Synonyms: 1-Amino-2-hydroxyindane, 422-660-2, 1-Amino-2-indanol, 74165-73-4, 1-amino-2,3-dihydro-1H-inden-2-ol

Application

1-Amino-2-hydroxyindane serves as a key chiral synthon in asymmetric synthesis of bioactive molecules, particularly in pharmaceutical intermediates. The compound’s rigid indane scaffold makes it valuable for developing dopamine receptor ligands and CNS-active compounds. Researchers utilize this building block for constructing chiral auxiliaries and catalysts in stereoselective transformations. Its bifunctional nature allows for diverse derivatization at both the amino and hydroxyl groups.

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