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Atomfair 6-Chloro-4-nitro-o-toluidine C7H7ClN2O2

Description 6-Chloro-4-nitro-o-toluidine (CAS No. 13852-51-2) is a high-purity nitroaromatic compound with the molecular formula C7H7ClN2O2and IUPAC name 5-chloro-2-methyl-4-nitroaniline . This fine chemical is characterized by its pale yellow to amber crystalline appearance and is widely utilized in synthetic organic chemistry and dye manufacturing. With a molecular weight of 186.60 g/mol, it exhibits excellent stability under standard laboratory conditions. Our product is rigorously tested for purity (typically ??98% by HPLC) and is supplied in sealed, light-resistant containers to ensure long-term integrity. Ideal for researchers requiring precise intermediates in heterocyclic synthesis or pigment development.

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Description

Description

6-Chloro-4-nitro-o-toluidine (CAS No. 13852-51-2) is a high-purity nitroaromatic compound with the molecular formula C7H7ClN2O2 and IUPAC name 5-chloro-2-methyl-4-nitroaniline. This fine chemical is characterized by its pale yellow to amber crystalline appearance and is widely utilized in synthetic organic chemistry and dye manufacturing. With a molecular weight of 186.60 g/mol, it exhibits excellent stability under standard laboratory conditions. Our product is rigorously tested for purity (typically ??98% by HPLC) and is supplied in sealed, light-resistant containers to ensure long-term integrity. Ideal for researchers requiring precise intermediates in heterocyclic synthesis or pigment development.

  • CAS No: 13852-51-2
  • Molecular Formula: C7H7ClN2O2
  • Molecular Weight: 186.59
  • Exact Mass: 186.0196052
  • Monoisotopic Mass: 186.0196052
  • IUPAC Name: 5-chloro-2-methyl-4-nitroaniline
  • SMILES: CC1=CC(=C(C=C1N)Cl)[N+](=O)[O-]
  • Synonyms: 13852-51-2, 6-Chloro-4-nitro-o-toluidine, EINECS 237-589-0, DTXSID30160702, NSC 60116

Application

6-Chloro-4-nitro-o-toluidine serves as a key intermediate in the synthesis of azo dyes and pigments, particularly for textile applications. It finds use in pharmaceutical research for building blocks in active pharmaceutical ingredient (API) development. The compound’s nitro and chloro functional groups make it valuable for electrophilic substitution reactions in advanced organic synthesis.

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