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CAS 131747-67-6

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5-Trifluoromethyl-pyridine-3-carbaldehyde

Description:
5-Trifluoromethyl-pyridine-3-carbaldehyde is an organic compound characterized by the presence of a pyridine ring substituted with a trifluoromethyl group and an aldehyde functional group. The trifluoromethyl group (-CF3) is known for its electron-withdrawing properties, which can significantly influence the reactivity and stability of the compound. The aldehyde functional group (-CHO) is reactive and can participate in various chemical reactions, including condensation and oxidation. This compound is typically a colorless to pale yellow liquid or solid, depending on its state at room temperature. It is soluble in organic solvents and may exhibit moderate volatility. Due to the presence of fluorine atoms, it may also display unique properties such as increased lipophilicity and altered boiling points compared to non-fluorinated analogs. 5-Trifluoromethyl-pyridine-3-carbaldehyde is of interest in medicinal chemistry and materials science, often serving as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Safety precautions should be taken when handling this compound, as it may pose health risks.
Formula:C7H4F3NO
InChI:InChI=1/C7H4F3NO/c8-7(9,10)6-1-5(4-12)2-11-3-6/h1-4H
SMILES:c1c(cncc1C(F)(F)F)C=O
Synonyms:
  • 3-Pyridinecarboxaldehyde, 5-(trifluoromethyl)-
  • 5-Trifluoromethyl-pyridine-3-carbaldehyde
  • 5-(trifluoromethyl)-3-Pyridinecarboxaldehyde
  • 5-(trifluoroMethyl)nicotinaldehyde
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