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CAS 1979-96-0

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4,6-dichloro-2-(methylthio)-5-nitropyrimidine

Description:
4,6-Dichloro-2-(methylthio)-5-nitropyrimidine is a heterocyclic organic compound characterized by its pyrimidine ring, which is substituted at the 4 and 6 positions with chlorine atoms, at the 2 position with a methylthio group, and at the 5 position with a nitro group. This compound is typically a solid at room temperature and exhibits a pale yellow to brown color. It is known for its potential applications in pharmaceuticals and agrochemicals, particularly as an intermediate in the synthesis of various biologically active compounds. The presence of chlorine and nitro groups contributes to its reactivity, making it useful in further chemical transformations. Additionally, the methylthio group can influence the compound's solubility and biological activity. As with many halogenated compounds, it is important to handle 4,6-dichloro-2-(methylthio)-5-nitropyrimidine with care due to potential toxicity and environmental concerns. Proper safety measures should be observed when working with this substance in laboratory or industrial settings.
Formula:C5H3Cl2N3O2S
InChI:InChI=1/C5H3Cl2N3O2S/c1-13-5-8-3(6)2(10(11)12)4(7)9-5/h1H3
SMILES:CSc1nc(c(c(Cl)n1)N(=O)=O)Cl
Synonyms:
  • 4,6-Dichloro-2-methylsulfanyl-5-nitro-pyrimidine
  • 4,6-Dichloro-2-(Methylthio)-5-nitropyriMidine
  • 4,6-Dichloro-2-Methylsulfanyl-5-nitro-pyriMidine-3
  • 2-Methylthio-4,6-dichloro-5-nitro-pyriMidine
  • 4,6-Dichloro-2-(methylthio)-5-nitropyrimidine 98%
  • 4,6-Dichloro-2-Methylsulfanyl-5-nitro-pyriMidine ISO 9001：2015 REACH
  • Pyrimidine, 4,6-dichloro-2-(methylthio)-5-nitro-
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