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Atomfair 2,4-Dinitrobenzaldehyde C7H4N2O5

Description 2,4-Dinitrobenzaldehyde (CAS No. 528-75-6) is a high-purity nitro-substituted benzaldehyde derivative with the molecular formula C7H4N2O5. This yellow crystalline solid is widely utilized in organic synthesis, pharmaceutical research, and as a key intermediate in the preparation of dyes, pigments, and specialty chemicals. Its IUPAC name is 2,4-dinitrobenzaldehyde , and it is characterized by its two nitro groups at the 2- and 4-positions, which enhance its reactivity in electrophilic and nucleophilic substitution reactions. Our product is rigorously tested for purity, ensuring optimal performance in sensitive applications. Store in a cool, dry place away from light and incompatible substances.

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Description

Description

2,4-Dinitrobenzaldehyde (CAS No. 528-75-6) is a high-purity nitro-substituted benzaldehyde derivative with the molecular formula C7H4N2O5. This yellow crystalline solid is widely utilized in organic synthesis, pharmaceutical research, and as a key intermediate in the preparation of dyes, pigments, and specialty chemicals. Its IUPAC name is 2,4-dinitrobenzaldehyde, and it is characterized by its two nitro groups at the 2- and 4-positions, which enhance its reactivity in electrophilic and nucleophilic substitution reactions. Our product is rigorously tested for purity, ensuring optimal performance in sensitive applications. Store in a cool, dry place away from light and incompatible substances.

  • CAS No: 528-75-6
  • Molecular Formula: C7H4N2O5
  • Molecular Weight: 196.12
  • Exact Mass: 196.01202123
  • Monoisotopic Mass: 196.01202123
  • IUPAC Name: 2,4-dinitrobenzaldehyde
  • SMILES: C1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])C=O
  • Synonyms: 2,4-Dinitrobenzaldehyde, 528-75-6, Benzaldehyde, 2,4-dinitro-, CCRIS 2684, UNII-ZAC919YU3Z

Application

2,4-Dinitrobenzaldehyde serves as a versatile building block in organic synthesis, particularly in the preparation of heterocyclic compounds and Schiff bases. It is employed in the synthesis of pharmaceuticals, agrochemicals, and dyes due to its electron-withdrawing nitro groups. Researchers also use it as a derivatization agent in analytical chemistry for the detection of amines and hydrazines. Its reactivity makes it valuable in photochemical studies and material science applications.

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