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CAS 54503-93-4

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4-chloro-6-piperidin-1-ylpyrimidine-5-carbaldehyde

Description:
4-Chloro-6-piperidin-1-ylpyrimidine-5-carbaldehyde is a chemical compound characterized by its pyrimidine core, which is a six-membered heterocyclic ring containing two nitrogen atoms. The presence of a chloro group at the 4-position and a piperidine moiety at the 6-position contributes to its unique reactivity and potential biological activity. The aldehyde functional group at the 5-position is significant for its reactivity, allowing for various chemical transformations, including condensation reactions. This compound may exhibit properties typical of both heterocycles and aldehydes, such as potential antimicrobial or anti-inflammatory activities, making it of interest in medicinal chemistry. Its structure suggests it could participate in interactions with biological targets, possibly influencing enzyme activity or receptor binding. Additionally, the presence of the piperidine ring may enhance its lipophilicity, affecting its pharmacokinetic properties. As with many synthetic organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.
Formula:C10H12ClN3O
InChI:InChI=1/C10H12ClN3O/c11-9-8(6-15)10(13-7-12-9)14-4-2-1-3-5-14/h6-7H,1-5H2
SMILES:C1CCN(CC1)c1c(C=O)c(Cl)ncn1
Synonyms:
  • 1-(6-Chloro-5-formylpyrimidin-4-yl)piperidine, 4-Chloro-6-(piperidin-1-yl)-1,3-diazine-5-carboxaldehyde
  • 4-CHLORO-6-PIPERIDINO-5-PYRIMIDINECARBALDEHYDE
  • 5-Pyrimidinecarboxaldehyde, 4-chloro-6-(1-piperidinyl)-
  • 4-chloro-6-piperidin-1-ylpyrimidine-5-carbaldehyde
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