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CAS 1192155-06-8

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Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate

Description:
Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate is a chemical compound characterized by its pyridazine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms. The presence of a trifluoromethyl group (-CF3) at the 6-position significantly influences its chemical properties, enhancing its lipophilicity and potentially its biological activity. The ethyl ester functional group contributes to its reactivity, making it amenable to various chemical transformations. This compound may exhibit interesting pharmacological properties, as many pyridazine derivatives are known for their diverse biological activities, including anti-inflammatory and antimicrobial effects. Its molecular structure suggests potential applications in medicinal chemistry and agrochemicals. Additionally, the trifluoromethyl group can enhance metabolic stability and influence the compound's interaction with biological targets. As with many fluorinated compounds, safety and environmental considerations are important, given the persistence of fluorinated substances in the environment. Overall, Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate represents a class of compounds with significant potential in various chemical and pharmaceutical applications.
Formula:C8H7F3N2O2
InChI:InChI=1S/C8H7F3N2O2/c1-2-15-7(14)5-3-4-6(13-12-5)8(9,10)11/h3-4H,2H2,1H3
InChI key:InChIKey=BLOPWFFYYJNVNZ-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1=CC=C(C(F)(F)F)N=N1
Synonyms:
  • Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate
  • 3-Pyridazinecarboxylic acid, 6-(trifluoromethyl)-, ethyl ester
  • Ethyl6-(trifluoromethyl)pyridazine-3-carboxylate ISO 9001：2015 REACH
  • Ethyl6-(trifluoromethyl)pyridazine-3-carboxylate
  • pyridazine-3-carboxylate
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