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CAS 6237-96-3

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4,6-Dichloro-2-ethyl-5-pyrimidinamine

Description:
4,6-Dichloro-2-ethyl-5-pyrimidinamine, with the CAS number 6237-96-3, is an organic compound belonging to the pyrimidine family. It features a pyrimidine ring substituted with two chlorine atoms at the 4 and 6 positions, an ethyl group at the 2 position, and an amino group at the 5 position. This compound is typically characterized by its solid state at room temperature and exhibits moderate solubility in polar solvents due to the presence of the amino group, which can engage in hydrogen bonding. The dichloro substitutions contribute to its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. Its structure suggests potential applications in pharmaceuticals, particularly as an intermediate in the synthesis of biologically active compounds. Additionally, the presence of chlorine atoms may impart specific properties such as increased lipophilicity or altered metabolic stability. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks.
Formula:C6H7Cl2N3
InChI:InChI=1S/C6H7Cl2N3/c1-2-3-10-5(7)4(9)6(8)11-3/h2,9H2,1H3
InChI key:InChIKey=IQHHPQSMYVIVOB-UHFFFAOYSA-N
SMILES:C(C)C=1N=C(Cl)C(N)=C(Cl)N1
Synonyms:
  • 2H-Pyrrol-2-one, 1,5-dihydro-3-hydroxy-5-(4-methylphenyl)-1-(1,3,4-thiadiazol-2-yl)-4-(2-thienylcarbonyl)-
  • 3-Hydroxy-5-(4-methylphenyl)-1-(1,3,4-thiadiazol-2-yl)-4-(2-thienylcarbonyl)-1,5-dihydro-2H-pyrrol-2-one
  • 4,6-Dichloro-2-ethyl-5-pyrimidinamine
  • 4,6-Dichloro-2-ethylpyrimidin-5-amine
  • 5-Pyrimidinamine, 4,6-dichloro-2-ethyl-
  • Pyrimidine, 5-amino-4,6-dichloro-2-ethyl-
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