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CAS 128073-05-2

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5-(Trifluoromethyl)-2-pyridinecarbonyl chloride

Description:
5-(Trifluoromethyl)-2-pyridinecarbonyl chloride is a chemical compound characterized by its unique structure, which includes a pyridine ring substituted with a trifluoromethyl group and a carbonyl chloride functional group. This compound is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is known for its reactivity, particularly due to the presence of the carbonyl chloride group, which can participate in nucleophilic substitution reactions. The trifluoromethyl group enhances the compound's lipophilicity and can influence its biological activity, making it of interest in medicinal chemistry and agrochemical applications. Additionally, this compound may exhibit moderate to high toxicity, necessitating careful handling and storage under appropriate safety protocols. Its applications can range from serving as an intermediate in organic synthesis to potential uses in the development of pharmaceuticals or agrochemicals. As with many halogenated compounds, it is important to consider environmental impacts and regulatory guidelines when working with or disposing of this substance.
Formula:C7H3ClF3NO
InChI:InChI=1S/C7H3ClF3NO/c8-6(13)5-2-1-4(3-12-5)7(9,10)11/h1-3H
InChI key:InChIKey=XGGHEBGOZWCTKF-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1C=CC(C(Cl)=O)=NC1
Synonyms:
  • 5-(Trifluoromethyl)-2-pyridinecarbonyl chloride
  • 5-Trifluoromethylpyridine-2-carbonyl chloride
  • 2-Pyridinecarbonyl chloride, 5-(trifluoromethyl)-
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