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CAS 1134327-91-5

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Ethyl 5-bromo-2-pyrimidineacetate

Description:
Ethyl 5-bromo-2-pyrimidineacetate is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a bromine atom at the 5-position of the pyrimidine ring contributes to its reactivity and potential applications in organic synthesis. The ethyl ester functional group, derived from acetic acid, enhances its solubility in organic solvents and may influence its biological activity. This compound is typically used in medicinal chemistry and research due to its potential as a building block for more complex molecules. Its properties include moderate stability under standard conditions, but it may be sensitive to moisture and light. The compound's reactivity can be attributed to the electrophilic nature of the bromine atom, making it suitable for nucleophilic substitution reactions. Overall, Ethyl 5-bromo-2-pyrimidineacetate is a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals.
Formula:C8H9BrN2O2
InChI:InChI=1S/C8H9BrN2O2/c1-2-13-8(12)3-7-10-4-6(9)5-11-7/h4-5H,2-3H2,1H3
InChI key:InChIKey=WJXDNGKSVNQDBZ-UHFFFAOYSA-N
SMILES:C(C(OCC)=O)C=1N=CC(Br)=CN1
Synonyms:
  • 2-Pyrimidineacetic acid, 5-bromo-, ethyl ester
  • Ethyl 2-(5-bromopyrimidin-2-yl)acetate
  • Ethyl 5-bromo-2-pyrimidineacetate
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