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CAS 10132-07-7

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2,6-Dichloro-4-pyrimidinamine

Description:
2,6-Dichloro-4-pyrimidinamine is an organic compound characterized by its pyrimidine ring structure, which features two chlorine atoms at the 2 and 6 positions and an amino group at the 4 position. This compound is typically a solid at room temperature and is known for its role as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It exhibits moderate solubility in polar solvents, which is influenced by the presence of the amino group that can engage in hydrogen bonding. The chlorine substituents contribute to its reactivity, making it a useful building block in chemical synthesis. Additionally, 2,6-Dichloro-4-pyrimidinamine may exhibit biological activity, which can be leveraged in medicinal chemistry. Safety data indicates that, like many chlorinated compounds, it should be handled with care due to potential toxicity and environmental concerns. Proper storage and disposal practices are essential to mitigate any risks associated with its use.
Formula:C4H3Cl2N3
InChI:InChI=1S/C4H3Cl2N3/c5-2-1-3(7)9-4(6)8-2/h1H,(H2,7,8,9)
InChI key:InChIKey=UPVBKNZVOJNQKE-UHFFFAOYSA-N
SMILES:ClC=1C=C(N)N=C(Cl)N1
Synonyms:
  • 2,4-Dichloro-6-Amino Pyrimidine
  • 2,4-Dichloro-6-aminopyrimidine
  • 2,6-Dichloro-4-aminopyrimidine
  • 2,6-Dichloro-4-pyrimidinamine
  • 2,6-Dichloropyrimidin-4-Amine
  • 2,6-Dichloropyrimidin-4-ylamine
  • 4-Pyrimidinamine, 2,6-dichloro-
  • 6-Amino-2,4-dichloropyrimidine
  • NSC 51667
  • Pyrimidine, 4-amino-2,6-dichloro-
  • 4-Amino-2,6-dichloropyrimidine
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