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Atomfair 4-Chloro-3,5-dinitrobenzamide C7H4ClN3O5

Description 4-Chloro-3,5-dinitrobenzamide (CAS No. 20731-63-9) is a high-purity nitroaromatic compound with the molecular formula C7H4ClN3O5. This yellow crystalline powder is a versatile intermediate in organic synthesis, particularly in the development of agrochemicals, pharmaceuticals, and specialty chemicals. With a molecular weight of 245.58 g/mol, it features both chloro and nitro functional groups, making it a valuable precursor for nucleophilic substitution and reduction reactions. Our product is rigorously tested for purity (typically ??95% by HPLC) and is supplied with full analytical documentation, including1H NMR and LC-MS spectra. Suitable for research-scale applications, it is packaged under inert atmosphere in amber glass vials to…

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Description

Description

4-Chloro-3,5-dinitrobenzamide (CAS No. 20731-63-9) is a high-purity nitroaromatic compound with the molecular formula C7H4ClN3O5. This yellow crystalline powder is a versatile intermediate in organic synthesis, particularly in the development of agrochemicals, pharmaceuticals, and specialty chemicals. With a molecular weight of 245.58 g/mol, it features both chloro and nitro functional groups, making it a valuable precursor for nucleophilic substitution and reduction reactions. Our product is rigorously tested for purity (typically ??95% by HPLC) and is supplied with full analytical documentation, including 1H NMR and LC-MS spectra. Suitable for research-scale applications, it is packaged under inert atmosphere in amber glass vials to ensure stability.

  • CAS No: 20731-63-9
  • Molecular Formula: C7H4ClN3O5
  • Molecular Weight: 245.58
  • Exact Mass: 244.9839479
  • Monoisotopic Mass: 244.9839479
  • IUPAC Name: 4-chloro-3,5-dinitrobenzamide
  • SMILES: C1=C(C=C(C(=C1[N+](=O)[O-])Cl)[N+](=O)[O-])C(=O)N
  • Synonyms: 4-Chloro-3,5-dinitrobenzamide, 20731-63-9, EINECS 243-998-5, DTXSID70174803, NSC 76582

Application

4-Chloro-3,5-dinitrobenzamide serves as a key intermediate in the synthesis of herbicidal compounds, particularly for crop protection agents targeting broadleaf weeds. Researchers utilize its reactive nitro groups for the development of novel sulfonylurea-class herbicides. In medicinal chemistry, it has been explored as a scaffold for antimicrobial agents due to its electrophilic aromatic substitution potential. The compound’s chlorine moiety also enables cross-coupling reactions in catalyst-driven organic transformations.

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