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Atomfair N-methyl-2-(4-methylpiperazin-1-yl)-N-(4-nitrophenyl)acetamide C14H20N4O3

Description N-methyl-2-(4-methylpiperazin-1-yl)-N-(4-nitrophenyl)acetamide (CAS No. 1139453-98-7) is a high-purity synthetic compound with the molecular formula C14H20N4O3. This specialized chemical features a unique molecular structure combining a methylpiperazine moiety with a nitrophenylacetamide group, making it a valuable intermediate for pharmaceutical research and organic synthesis. The compound is supplied as a solid with ??95% purity (HPLC), rigorously tested for quality assurance including NMR, LC-MS, and elemental analysis. Proper storage at 2-8??C in a tightly sealed container under inert atmosphere is recommended for long-term stability. Researchers should handle this material with appropriate PPE due to its potential reactivity.

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Description

Description

N-methyl-2-(4-methylpiperazin-1-yl)-N-(4-nitrophenyl)acetamide (CAS No. 1139453-98-7) is a high-purity synthetic compound with the molecular formula C14H20N4O3. This specialized chemical features a unique molecular structure combining a methylpiperazine moiety with a nitrophenylacetamide group, making it a valuable intermediate for pharmaceutical research and organic synthesis. The compound is supplied as a solid with ??95% purity (HPLC), rigorously tested for quality assurance including NMR, LC-MS, and elemental analysis. Proper storage at 2-8??C in a tightly sealed container under inert atmosphere is recommended for long-term stability. Researchers should handle this material with appropriate PPE due to its potential reactivity.

  • CAS No: 1139453-98-7
  • Molecular Formula: C14H20N4O3
  • Molecular Weight: 292.33
  • Exact Mass: 292.15354051
  • Monoisotopic Mass: 292.15354051
  • IUPAC Name: N-methyl-2-(4-methylpiperazin-1-yl)-N-(4-nitrophenyl)acetamide
  • SMILES: CN1CCN(CC1)CC(=O)N(C)C2=CC=C(C=C2)[N+](=O)[O-]
  • Synonyms: 1139453-98-7, N-methyl-2-(4-methylpiperazin-1-yl)-N-(4-nitrophenyl)acetamide, DTXSID00634602, DTXCID70585354, 813-785-7

Application

This compound serves as a key building block in medicinal chemistry research, particularly for developing novel kinase inhibitors and CNS-active pharmaceuticals. Its structural features make it valuable for structure-activity relationship (SAR) studies in drug discovery programs. The nitrophenyl group provides opportunities for further chemical modifications through reduction or substitution reactions.

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