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Atomfair Methyl 2-chloro-4-nitrobenzoate C8H6ClNO4

Description Methyl 2-chloro-4-nitrobenzoate (CAS No. 13324-11-3) is a high-purity organic compound with the molecular formula C8H6ClNO4. This aromatic ester is characterized by its chloro and nitro functional groups at the 2- and 4-positions of the benzoate ring, respectively, making it a versatile intermediate in synthetic organic chemistry. It is supplied as a crystalline solid with a consistent purity of ??98% (HPLC), ensuring reliability for research and industrial applications. Ideal for use in pharmaceutical synthesis , agrochemical development , and material science , this compound is packaged under inert conditions to maintain stability. Available in quantities ranging from grams to kilograms,…

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Description

Description

Methyl 2-chloro-4-nitrobenzoate (CAS No. 13324-11-3) is a high-purity organic compound with the molecular formula C8H6ClNO4. This aromatic ester is characterized by its chloro and nitro functional groups at the 2- and 4-positions of the benzoate ring, respectively, making it a versatile intermediate in synthetic organic chemistry. It is supplied as a crystalline solid with a consistent purity of ??98% (HPLC), ensuring reliability for research and industrial applications. Ideal for use in pharmaceutical synthesis, agrochemical development, and material science, this compound is packaged under inert conditions to maintain stability. Available in quantities ranging from grams to kilograms, it is suitable for both laboratory-scale experiments and bulk manufacturing.

  • CAS No: 13324-11-3
  • Molecular Formula: C8H6ClNO4
  • Molecular Weight: 215.59
  • Exact Mass: 214.9985354
  • Monoisotopic Mass: 214.9985354
  • IUPAC Name: methyl 2-chloro-4-nitrobenzoate
  • SMILES: COC(=O)C1=C(C=C(C=C1)[N+](=O)[O-])Cl
  • Synonyms: Methyl 2-chloro-4-nitrobenzoate, Benzoic acid, 2-chloro-4-nitro-, methyl ester, 2-Chloro-4-nitrobenzoic Acid Methyl Ester, F9KQ5NY29Z, EINECS 236-362-3

Application

Methyl 2-chloro-4-nitrobenzoate is widely employed as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with nitro-aromatic scaffolds. Its reactive sites make it valuable for cross-coupling reactions and nucleophilic substitutions in agrochemical research. Additionally, it serves as a precursor for dyes and advanced materials due to its electron-withdrawing nitro group.

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