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Atomfair 1,3-Dimethyl-5-nitrobenzene 5-Nitro-m-xylene C8H9NO2

Description 1,3-Dimethyl-5-nitrobenzene (CAS No. 2106-04-9) is a high-purity nitroaromatic compound with the molecular formula C8H9NO2. This yellow crystalline solid is a valuable intermediate in organic synthesis, particularly in the production of dyes, pharmaceuticals, and agrochemicals. With an IUPAC name of 1,3-dimethyl-5-nitrobenzene , it is also known by synonyms such as 5-Nitro-m-xylene and 5-Methyl-3-nitrotoluene . Our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed containers to maintain stability. Ideal for researchers in fine chemical synthesis, this compound offers excellent reactivity for electrophilic aromatic substitution and reduction reactions. Store in a cool, dry place away from…

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Description

Description

1,3-Dimethyl-5-nitrobenzene (CAS No. 2106-04-9) is a high-purity nitroaromatic compound with the molecular formula C8H9NO2. This yellow crystalline solid is a valuable intermediate in organic synthesis, particularly in the production of dyes, pharmaceuticals, and agrochemicals. With an IUPAC name of 1,3-dimethyl-5-nitrobenzene, it is also known by synonyms such as 5-Nitro-m-xylene and 5-Methyl-3-nitrotoluene. Our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed containers to maintain stability. Ideal for researchers in fine chemical synthesis, this compound offers excellent reactivity for electrophilic aromatic substitution and reduction reactions. Store in a cool, dry place away from strong oxidizers.

  • CAS No: 2106-04-9
  • Molecular Formula: C8H9NO2
  • Molecular Weight: 151.16
  • Exact Mass: 151.063328530
  • Monoisotopic Mass: 151.063328530
  • IUPAC Name: 1,3-dimethyl-5-nitrobenzene
  • SMILES: CC1=CC(=CC(=C1)[N+](=O)[O-])C
  • Synonyms: 5-Nitro-m-xylene, 1,3-DIMETHYL-5-NITROBENZENE, 99-12-7, CCRIS 3121, 5-Methyl-3-nitrotoluene

Application

1,3-Dimethyl-5-nitrobenzene serves as a key precursor in the synthesis of specialty chemicals, including azo dyes and pharmaceutical intermediates. Its nitro group facilitates catalytic hydrogenation to yield aromatic amines for polymer production. Researchers also utilize it in electrophilic substitution studies due to the electron-withdrawing nitro group’s influence on the benzene ring’s reactivity. In agrochemical development, it acts as a building block for herbicides and fungicides.

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