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CAS 63155-10-2

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Ethyl 4,6-dichloro-2-pyrimidineacetate

Description:
Ethyl 4,6-dichloro-2-pyrimidineacetate is a chemical compound characterized by its pyrimidine ring structure, which is substituted at the 4 and 6 positions with chlorine atoms. This compound features an ethyl ester functional group, contributing to its reactivity and solubility properties. Typically, compounds of this nature exhibit moderate to high stability under standard conditions, but they may be sensitive to hydrolysis, particularly in the presence of strong acids or bases. Ethyl 4,6-dichloro-2-pyrimidineacetate is often utilized in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its chlorinated pyrimidine structure can impart biological activity, making it of interest in medicinal chemistry. Safety data sheets should be consulted for handling and storage guidelines, as halogenated compounds can pose environmental and health risks. Overall, this compound exemplifies the diverse applications of pyrimidine derivatives in chemical research and industry.
Formula:C8H8Cl2N2O2
InChI:InChI=1S/C8H8Cl2N2O2/c1-2-14-8(13)4-7-11-5(9)3-6(10)12-7/h3H,2,4H2,1H3
InChI key:InChIKey=BVWJBJVHLJIVST-UHFFFAOYSA-N
SMILES:C(C(OCC)=O)C=1N=C(Cl)C=C(Cl)N1
Synonyms:
  • 2-Pyrimidineacetic acid, 4,6-dichloro-, ethyl ester
  • Ethyl 4,6-dichloro-2-pyrimidineacetate
  • Ethyl 2-(4,6-dichloropyriMidin-2-yl)-acetate
  • ethyl 2-(4,6-dichloropyrimidin-2-yl)acetate/63155-10-2
  • 4,6-Dichloro-2-pyrimidineacetic acid ethyl ester
  • Ethyl 2-(4,6-dichloropyrimidin-2-yl)
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