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CAS 505084-57-1

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2-Chloro-5-(trifluoromethyl)-4-pyridinecarboxaldehyde

Description:
2-Chloro-5-(trifluoromethyl)-4-pyridinecarboxaldehyde is a chemical compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. The presence of a chloro group at the 2-position and a trifluoromethyl group at the 5-position significantly influences its chemical properties, including its reactivity and polarity. The aldehyde functional group at the 4-position contributes to its potential as a reactive intermediate in organic synthesis. This compound is typically used in the synthesis of various pharmaceuticals and agrochemicals due to its unique electronic properties and ability to participate in nucleophilic addition reactions. It is important to handle this substance with care, as it may pose health risks, including irritation to the skin and eyes, and potential toxicity if ingested or inhaled. Proper safety protocols should be followed when working with this compound in a laboratory setting.
Formula:C7H3ClF3NO
InChI:InChI=1S/C7H3ClF3NO/c8-6-1-4(3-13)5(2-12-6)7(9,10)11/h1-3H
InChI key:InChIKey=TUIUCTUSVSDRSW-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1C(C=O)=CC(Cl)=NC1
Synonyms:
  • 2-Chloro-5-(trifluoromethyl)-4-pyridinecarboxaldehyde
  • 2-Chloro-5-(trifluoromethyl)isonicotinaldehyde
  • 4-Pyridinecarboxaldehyde, 2-Chloro-5-(Trifluoromethyl)-
  • 2-Chloro-5-(trifluoromethyl)pyridine-4-carbaldehyde
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