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CAS 350997-70-5

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5-Chloro-3-methyl-1-(p-tolyl)-1H-pyrazole-4-carboxaldehyde

Description:
5-Chloro-3-methyl-1-(p-tolyl)-1H-pyrazole-4-carboxaldehyde is an organic compound characterized by its pyrazole ring structure, which is a five-membered heterocyclic compound containing two nitrogen atoms. The presence of a chloro group at the 5-position and a methyl group at the 3-position contributes to its unique reactivity and physical properties. The p-tolyl group, a para-substituted phenyl group, enhances its lipophilicity and may influence its biological activity. The aldehyde functional group at the 4-position is reactive, making the compound useful in various synthetic applications, including as an intermediate in the synthesis of pharmaceuticals or agrochemicals. This compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its chemical behavior can be influenced by the electron-withdrawing nature of the chloro group and the electron-donating characteristics of the methyl and p-tolyl groups, which can affect its reactivity in nucleophilic addition reactions. Overall, this compound is of interest in medicinal chemistry and material science due to its structural features and potential applications.
Formula:C12H11ClN2O
InChI:InChI=1/C12H11ClN2O/c1-8-3-5-10(6-4-8)15-12(13)11(7-16)9(2)14-15/h3-7H,1-2H3
SMILES:Cc1ccc(cc1)n1c(c(C=O)c(C)n1)Cl
Synonyms:
  • 5-chloro-3-methyl-1-(4-methylphenyl)-1H-pyrazole-4-carbaldehyde
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