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CAS 175137-15-2

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1-Phenyl-5-propyl-1H-pyrazole-4-carbonyl chloride

Description:
1-Phenyl-5-propyl-1H-pyrazole-4-carbonyl chloride is a chemical compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features a phenyl group and a propyl group attached to the pyrazole, contributing to its unique properties and reactivity. The presence of the carbonyl chloride functional group indicates that it is a reactive acyl chloride, making it useful in various synthetic applications, particularly in the formation of amides and esters. The compound's molecular structure suggests potential applications in medicinal chemistry, possibly as a precursor for biologically active molecules. Its reactivity is influenced by the electron-withdrawing nature of the carbonyl chloride, which can facilitate nucleophilic attack. Additionally, the presence of both aromatic and aliphatic components in its structure may impart distinct physical properties, such as solubility and melting point, which are important for its handling and application in laboratory settings. Safety precautions should be taken due to the reactivity of the carbonyl chloride group.
Formula:C13H13ClN2O
InChI:InChI=1S/C13H13ClN2O/c1-2-6-12-11(13(14)17)9-15-16(12)10-7-4-3-5-8-10/h3-5,7-9H,2,6H2,1H3
InChI key:InChIKey=WGSJOUNRMCLMHQ-UHFFFAOYSA-N
SMILES:C(CC)C=1N(N=CC1C(Cl)=O)C2=CC=CC=C2
Synonyms:
  • 1-Phenyl-5-(n-propyl)pyrazole-4-carbonyl chloride
  • 1-Phenyl-5-propyl-4-pyrazolecarbonyl chloride
  • 1H-Pyrazole-4-carbonyl chloride, 1-phenyl-5-propyl-
  • 2-Phenyl-3-n-propylpyrazole-4-carbonyl chloride
  • 1-Phenyl-5-propyl-1H-pyrazole-4-carbonyl chloride
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