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Atomfair 4(3H)-Pyrimidinone, 6-hydroxy-5-nitro- C4H3N3O4

Description 4(3H)-Pyrimidinone, 6-hydroxy-5-nitro- (CAS No. 2164-83-2) is a high-purity heterocyclic organic compound with the molecular formula C4H3N3O4. This nitro-substituted pyrimidinone derivative is a valuable building block in pharmaceutical and biochemical research, particularly in the synthesis of nucleoside analogs and enzyme inhibitors. The compound features a reactive 4-hydroxy-5-nitro-1H-pyrimidin-6-one core structure, making it suitable for further functionalization and cross-coupling reactions. Our product is rigorously tested for purity (typically ??95% by HPLC) and is supplied as a fine, crystalline powder with excellent batch-to-batch consistency. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability.

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Description

Description

4(3H)-Pyrimidinone, 6-hydroxy-5-nitro- (CAS No. 2164-83-2) is a high-purity heterocyclic organic compound with the molecular formula C4H3N3O4. This nitro-substituted pyrimidinone derivative is a valuable building block in pharmaceutical and biochemical research, particularly in the synthesis of nucleoside analogs and enzyme inhibitors. The compound features a reactive 4-hydroxy-5-nitro-1H-pyrimidin-6-one core structure, making it suitable for further functionalization and cross-coupling reactions. Our product is rigorously tested for purity (typically ??95% by HPLC) and is supplied as a fine, crystalline powder with excellent batch-to-batch consistency. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability.

  • CAS No: 2164-83-2
  • Molecular Formula: C4H3N3O4
  • Molecular Weight: 157.08
  • Exact Mass: 157.01235559
  • Monoisotopic Mass: 157.01235559
  • IUPAC Name: 4-hydroxy-5-nitro-1H-pyrimidin-6-one
  • SMILES: C1=NC(=C(C(=O)N1)[N+](=O)[O-])O
  • Synonyms: 2164-83-2, 5-Nitropyrimidine-4,6-diol, 4(1H)-Pyrimidinone, 6-hydroxy-5-nitro-, 5-Nitro-4,6-dihydroxypyrimidine, 6-Hydroxy-5-nitro-4(1H)-pyrimidinone

Application

This nitro-substituted pyrimidinone serves as a key intermediate in medicinal chemistry for developing antiviral and anticancer agents. Researchers utilize it in the synthesis of modified nucleosides that mimic natural substrates for enzyme inhibition studies. The compound’s nitro group also makes it valuable for photoaffinity labeling applications in proteomics research.

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