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Atomfair 3′-Nitropropiophenone m-Nitropropiophenone C9H9NO3

Description 3′-Nitropropiophenone (CAS No. 17408-16-1) is a high-purity organic compound with the molecular formula C9H9NO3and IUPAC name 1-(3-nitrophenyl)propan-1-one. This aromatic ketone features a nitro group at the meta position of the phenyl ring, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. With a molecular weight of 179.17 g/mol, it is typically supplied as a crystalline solid with >98% purity (HPLC), ensuring consistency for demanding applications. Ideal for use in Grignard reactions, Friedel-Crafts acylations, and as a precursor for fine chemicals. Store in a cool, dry place away from light and oxidizing agents.

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Description

Description

3′-Nitropropiophenone (CAS No. 17408-16-1) is a high-purity organic compound with the molecular formula C9H9NO3 and IUPAC name 1-(3-nitrophenyl)propan-1-one. This aromatic ketone features a nitro group at the meta position of the phenyl ring, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. With a molecular weight of 179.17 g/mol, it is typically supplied as a crystalline solid with >98% purity (HPLC), ensuring consistency for demanding applications. Ideal for use in Grignard reactions, Friedel-Crafts acylations, and as a precursor for fine chemicals. Store in a cool, dry place away from light and oxidizing agents.

  • CAS No: 17408-16-1
  • Molecular Formula: C9H9NO3
  • Molecular Weight: 179.17
  • Exact Mass: 179.058243149
  • Monoisotopic Mass: 179.058243149
  • IUPAC Name: 1-(3-nitrophenyl)propan-1-one
  • SMILES: CCC(=O)C1=CC(=CC=C1)[N+](=O)[O-]
  • Synonyms: 3′-Nitropropiophenone, 17408-16-1, m-Nitropropiophenone, 1-Propanone, 1-(3-nitrophenyl)-, 2H7AZ76A5R

Application

3′-Nitropropiophenone is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. It serves as a precursor for the preparation of ??-amino ketones and other nitro-aromatic derivatives. Researchers utilize this compound in organic synthesis, particularly in reactions involving nucleophilic substitution or reduction of the nitro group. Its structural features make it valuable for studying reaction mechanisms and developing novel compounds with potential biological activity.

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