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CAS 175137-14-1

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1-Phenyl-5-(trifluoromethyl)-1H-pyrazole-4-carbonyl chloride

Description:
1-Phenyl-5-(trifluoromethyl)-1H-pyrazole-4-carbonyl chloride is a chemical compound characterized by its unique structure, which includes a pyrazole ring substituted with a phenyl group and a trifluoromethyl group. This compound features a carbonyl chloride functional group, making it a reactive acyl chloride. The presence of the trifluoromethyl group enhances its lipophilicity and can influence its reactivity and biological activity. Typically, compounds like this are of interest in medicinal chemistry and agrochemicals due to their potential as intermediates in the synthesis of pharmaceuticals or agrochemical agents. The compound is likely to be a solid at room temperature, with properties such as solubility in organic solvents. Its reactivity as an acyl chloride suggests it can participate in nucleophilic acyl substitution reactions, making it useful for further chemical transformations. Safety precautions should be taken when handling this compound, as acyl chlorides can be corrosive and may release harmful gases upon reaction with water or moisture.
Formula:C11H6ClF3N2O
InChI:InChI=1S/C11H6ClF3N2O/c12-10(18)8-6-16-17(9(8)11(13,14)15)7-4-2-1-3-5-7/h1-6H
InChI key:InChIKey=FSZPLNSWCMTQRJ-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1N(N=CC1C(Cl)=O)C2=CC=CC=C2
Synonyms:
  • 1-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carbonyl chloride
  • 1-Phenyl-5-(trifluoromethyl)-1H-pyrazole-4-carbonyl chloride
  • 1H-Pyrazole-4-carbonyl chloride, 1-phenyl-5-(trifluoromethyl)-
  • 1-Phenyl-5-(trifluoromethyl)pyrazole-4-carbonyl chloride
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