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CAS 130129-58-7

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5-Chloro-6-ethylpyrimidin-4-ol

Description:
5-Chloro-6-ethylpyrimidin-4-ol is a heterocyclic organic compound characterized by a pyrimidine ring substituted with a chlorine atom and an ethyl group, along with a hydroxyl group at the 4-position. This compound typically exhibits properties associated with pyrimidines, such as being a weak base due to the nitrogen atoms in the ring. The presence of the hydroxyl group contributes to its potential solubility in polar solvents and may influence its reactivity, particularly in nucleophilic substitution reactions. The chlorine substituent can enhance the compound's biological activity, making it of interest in pharmaceutical research. Additionally, the ethyl group can affect the compound's lipophilicity, impacting its absorption and distribution in biological systems. Overall, 5-Chloro-6-ethylpyrimidin-4-ol is notable for its structural features that may confer specific pharmacological properties, making it a subject of study in medicinal chemistry and related fields.
Formula:C6H7ClN2O
InChI:InChI=1/C6H7ClN2O/c1-2-4-5(7)6(10)9-3-8-4/h3H,2H2,1H3,(H,8,9,10)
SMILES:CCc1c(c(ncn1)O)Cl
Synonyms:
  • 5-Chloro-6-ethyl-4(1H)-pyrimidinone
  • 5-Chloro-6-ethyl-4-hydroxypyrimidine
  • 5-chloro-6-ethylpyrimidin-4(1H)-one
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