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Atomfair Methyl 2,4-dinitrobenzoate C8H6N2O6

Description Methyl 2,4-dinitrobenzoate (CAS No. 2702-58-1) is a high-purity nitroaromatic ester with the molecular formula C8H6N2O6. This compound is widely utilized in organic synthesis, pharmaceutical research, and material science due to its reactive nitro functional groups and ester moiety. It appears as a crystalline solid with a pale yellow to off-white coloration, offering excellent stability under standard laboratory conditions. Suitable for use as an intermediate in the preparation of dyes, agrochemicals, and specialty polymers, this reagent is rigorously tested for purity (typically ??97% by HPLC or GC analysis) and is supplied in sealed packaging to ensure integrity. Store in a…

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Description

Description

Methyl 2,4-dinitrobenzoate (CAS No. 2702-58-1) is a high-purity nitroaromatic ester with the molecular formula C8H6N2O6. This compound is widely utilized in organic synthesis, pharmaceutical research, and material science due to its reactive nitro functional groups and ester moiety. It appears as a crystalline solid with a pale yellow to off-white coloration, offering excellent stability under standard laboratory conditions. Suitable for use as an intermediate in the preparation of dyes, agrochemicals, and specialty polymers, this reagent is rigorously tested for purity (typically ??97% by HPLC or GC analysis) and is supplied in sealed packaging to ensure integrity. Store in a cool, dry place away from oxidizing agents and strong bases.

  • CAS No: 2702-58-1
  • Molecular Formula: C8H6N2O6
  • Molecular Weight: 226.14
  • Exact Mass: 226.02258592
  • Monoisotopic Mass: 226.02258592
  • IUPAC Name: methyl 2,4-dinitrobenzoate
  • SMILES: COC(=O)C1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]
  • Synonyms: Methyl 2,4-dinitrobenzoate, 18959-17-6, Benzoic acid, 2,4-dinitro-, methyl ester, Benzoic acid, 2,4-diniro-, methyl ester, SCHEMBL6960199

Application

Methyl 2,4-dinitrobenzoate serves as a versatile building block in the synthesis of nitroaromatic derivatives for pharmaceutical and agrochemical applications. Its electron-withdrawing nitro groups facilitate nucleophilic substitution reactions, making it valuable in the development of energetic materials and dyes. Researchers also employ it as a precursor in polymer modification and crosslinking studies due to its reactive ester functionality.

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