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CAS 21487-49-0

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3-(4-Nitrophenyl)-1-phenyl-1H-pyrazole-4-carboxaldehyde

Description:
3-(4-Nitrophenyl)-1-phenyl-1H-pyrazole-4-carboxaldehyde is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features a carboxaldehyde functional group (-CHO) at the 4-position of the pyrazole, contributing to its reactivity and potential applications in organic synthesis. The presence of a 4-nitrophenyl group enhances its electronic properties, making it useful in various chemical reactions, including nucleophilic substitutions and condensation reactions. The compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its nitro group can participate in electrophilic aromatic substitution reactions, while the aldehyde group can undergo oxidation or condensation reactions. This compound may be of interest in medicinal chemistry and materials science due to its potential biological activity and utility in the development of new pharmaceuticals or agrochemicals. Safety precautions should be taken when handling this compound, as it may pose health risks typical of nitro-substituted aromatic compounds.
Formula:C16H11N3O3
InChI:InChI=1/C16H11N3O3/c20-11-13-10-18(14-4-2-1-3-5-14)17-16(13)12-6-8-15(9-7-12)19(21)22/h1-11H
InChI key:InChIKey=CUVWNYMQNJNFGB-UHFFFAOYSA-N
SMILES:C(=O)C=1C(=NN(C1)C2=CC=CC=C2)C3=CC=C(N(=O)=O)C=C3
Synonyms:
  • 1H-Pyrazole-4-carboxaldehyde, 3-(4-nitrophenyl)-1-phenyl-
  • 3-(4-Nitro-phenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde
  • 3-(4-Nitrophenyl)-1-phenyl-1H-pyrazole-4-carboxaldehyde
  • 3-(4-Nitrophenyl)-1-phenylpyrazole-4-carboxaldehyde
  • Pyrazole-4-carboxaldehyde, 3-(p-nitrophenyl)-1-phenyl-
  • 3-(4-Nitrophenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde
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