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Atomfair 2-Amino-4-nitrobenzyl alcohol C7H8N2O3

Description 2-Amino-4-nitrobenzyl alcohol (CAS No. 78468-34-5) is a high-purity nitroaromatic compound with the molecular formula C7H8N2O3, widely utilized in organic synthesis and pharmaceutical research. This yellow to orange crystalline solid (IUPAC name: (2-amino-4-nitrophenyl)methanol) exhibits dual functional groups (-NH2and -NO2) on its benzene ring, making it a versatile intermediate for heterocyclic compound synthesis. Our HPLC-grade product undergoes rigorous QC testing including1H/13C NMR, FTIR, and mass spectrometry verification to ensure ??98% purity. Packaged under inert gas in amber glass vials with PTFE-lined caps to prevent degradation. Suitable for Suzuki coupling reactions, azo dye synthesis, and as a precursor for antimicrobial agents. SDS…

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Description

Description

2-Amino-4-nitrobenzyl alcohol (CAS No. 78468-34-5) is a high-purity nitroaromatic compound with the molecular formula C7H8N2O3, widely utilized in organic synthesis and pharmaceutical research. This yellow to orange crystalline solid (IUPAC name: (2-amino-4-nitrophenyl)methanol) exhibits dual functional groups (-NH2 and -NO2) on its benzene ring, making it a versatile intermediate for heterocyclic compound synthesis. Our HPLC-grade product undergoes rigorous QC testing including 1H/13C NMR, FTIR, and mass spectrometry verification to ensure ??98% purity. Packaged under inert gas in amber glass vials with PTFE-lined caps to prevent degradation. Suitable for Suzuki coupling reactions, azo dye synthesis, and as a precursor for antimicrobial agents. SDS and CoA available upon request.

  • CAS No: 78468-34-5
  • Molecular Formula: C7H8N2O3
  • Molecular Weight: 168.15
  • Exact Mass: 168.05349212
  • Monoisotopic Mass: 168.05349212
  • IUPAC Name: (2-amino-4-nitrophenyl)methanol
  • SMILES: C1=CC(=C(C=C1[N+](=O)[O-])N)CO
  • Synonyms: 2-AMINO-4-NITROBENZENEMETHANOL, 2-Amino-4-nitrobenzyl alcohol, 687-957-3, 78468-34-5, (2-amino-4-nitrophenyl)methanol

Application

2-Amino-4-nitrobenzyl alcohol serves as a key intermediate in the synthesis of benzimidazole derivatives with potential antimicrobial activity. Researchers employ this compound in the development of azo dyes for textile and biomedical staining applications due to its chromophoric nitro group. The material finds use in coordination chemistry as a bidentate ligand for transition metal complexes, particularly in catalytic systems.

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