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CAS 914636-56-9

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2,6-Dichloro-4-(trifluoromethyl)-3-pyridinecarboxaldehyde

Description:
2,6-Dichloro-4-(trifluoromethyl)-3-pyridinecarboxaldehyde is a chemical compound characterized by its pyridine ring, which is substituted at the 2 and 6 positions with chlorine atoms and at the 4 position with a trifluoromethyl group. The presence of the aldehyde functional group at the 3 position contributes to its reactivity, making it useful in various synthetic applications. This compound is typically a solid at room temperature and may exhibit a pale yellow to light brown color. It is known for its potential use in pharmaceuticals and agrochemicals due to its unique electronic properties imparted by the trifluoromethyl group, which enhances lipophilicity and biological activity. Additionally, the dichloro substituents can influence its chemical stability and reactivity. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 2,6-Dichloro-4-(trifluoromethyl)-3-pyridinecarboxaldehyde is a valuable compound in organic synthesis and medicinal chemistry.
Formula:C7H2Cl2F3NO
InChI:InChI=1S/C7H2Cl2F3NO/c8-5-1-4(7(10,11)12)3(2-14)6(9)13-5/h1-2H
InChI key:InChIKey=OBHMPLQCNUGZLV-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1C(C=O)=C(Cl)N=C(Cl)C1
Synonyms:
  • 2,6-Dichloro-4-(trifluoromethyl)-3-pyridinecarboxaldehyde
  • 3-Pyridinecarboxaldehyde, 2,6-dichloro-4-(trifluoromethyl)-
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