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Atomfair 3,5-Dinitrobenzonitrile C7H3N3O4

Description 3,5-Dinitrobenzonitrile (CAS No. 4110-35-4) is a high-purity nitroaromatic compound with the molecular formula C7H3N3O4. This yellow crystalline powder is widely utilized in organic synthesis, pharmaceutical research, and material science due to its reactive nitro and cyano functional groups. With an IUPAC name of 3,5-dinitrobenzonitrile , it is characterized by its excellent stability and compatibility with various chemical transformations. Our product is rigorously tested for purity (??98% by HPLC) and is supplied in sealed, light-resistant packaging to ensure long-term stability. Ideal for researchers seeking a versatile intermediate for electrophilic substitution reactions, nucleophilic aromatic substitutions, or as a precursor for agrochemicals…

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Description

Description

3,5-Dinitrobenzonitrile (CAS No. 4110-35-4) is a high-purity nitroaromatic compound with the molecular formula C7H3N3O4. This yellow crystalline powder is widely utilized in organic synthesis, pharmaceutical research, and material science due to its reactive nitro and cyano functional groups. With an IUPAC name of 3,5-dinitrobenzonitrile, it is characterized by its excellent stability and compatibility with various chemical transformations. Our product is rigorously tested for purity (??98% by HPLC) and is supplied in sealed, light-resistant packaging to ensure long-term stability. Ideal for researchers seeking a versatile intermediate for electrophilic substitution reactions, nucleophilic aromatic substitutions, or as a precursor for agrochemicals and dyes.

  • CAS No: 4110-35-4
  • Molecular Formula: C7H3N3O4
  • Molecular Weight: 193.12
  • Exact Mass: 193.01235559
  • Monoisotopic Mass: 193.01235559
  • IUPAC Name: 3,5-dinitrobenzonitrile
  • SMILES: C1=C(C=C(C=C1[N+](=O)[O-])[N+](=O)[O-])C#N
  • Synonyms: 3,5-Dinitrobenzonitrile, BENZONITRILE, 3,5-DINITRO-, EINECS 223-889-9, DTXSID60194050, NSC 35873

Application

3,5-Dinitrobenzonitrile serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its electron-withdrawing nitro and cyano groups make it valuable in nucleophilic aromatic substitution reactions for constructing complex heterocycles. Researchers also employ it as a precursor in the development of energetic materials and corrosion inhibitors. Additionally, it finds use in analytical chemistry as a derivatization agent for detection methods.

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