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Atomfair N-(3-nitrophenyl)acrylamide C9H8N2O3

Description N-(3-Nitrophenyl)acrylamide (CAS No. 17090-15-2) is a high-purity nitro-substituted acrylamide derivative with the molecular formula C9H8N2O3. This compound, also known by its IUPAC name N-(3-nitrophenyl)prop-2-enamide , features an acrylamide group bonded to a meta-nitrophenyl ring, making it a valuable intermediate for organic synthesis and polymer chemistry. With a molecular weight of 192.17 g/mol, it is supplied as a crystalline solid with ??95% purity (HPLC) and is ideal for electrophilic reactions, photo-crosslinking applications, and as a monomer for functionalized polymers. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability. Suitable for research and industrial applications requiring…

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Description

Description

N-(3-Nitrophenyl)acrylamide (CAS No. 17090-15-2) is a high-purity nitro-substituted acrylamide derivative with the molecular formula C9H8N2O3. This compound, also known by its IUPAC name N-(3-nitrophenyl)prop-2-enamide, features an acrylamide group bonded to a meta-nitrophenyl ring, making it a valuable intermediate for organic synthesis and polymer chemistry. With a molecular weight of 192.17 g/mol, it is supplied as a crystalline solid with ??95% purity (HPLC) and is ideal for electrophilic reactions, photo-crosslinking applications, and as a monomer for functionalized polymers. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability. Suitable for research and industrial applications requiring nitroaromatic acrylamides.

  • CAS No: 17090-15-2
  • Molecular Formula: C9H8N2O3
  • Molecular Weight: 192.17
  • Exact Mass: 192.05349212
  • Monoisotopic Mass: 192.05349212
  • IUPAC Name: N-(3-nitrophenyl)prop-2-enamide
  • SMILES: C=CC(=O)NC1=CC(=CC=C1)[N+](=O)[O-]
  • Synonyms: N-(3-nitrophenyl)acrylamide, 17090-15-2, 3-nitro-N-acrylphenylamine, N-(3-NITROPHENYL)PROP-2-ENAMIDE, MFCD00595891

Application

N-(3-Nitrophenyl)acrylamide serves as a key building block in the synthesis of photoactive polymers and nitroaromatic-functionalized materials. It is used in radical polymerization reactions to create stimuli-responsive hydrogels and coatings. Researchers employ this compound in click chemistry and as a precursor for pharmaceutical intermediates. Its nitro group enables further functionalization via reduction to amines or participation in nucleophilic aromatic substitution.

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