6-(2,2,2-Trifluoroethoxy)pyridine-3-carbaldehyde is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of the trifluoroethoxy group introduces significant electronegativity due to the three fluorine atoms, which can influence the compound's reactivity and polarity. This compound features an aldehyde functional group (-CHO) at the 3-position of the pyridine ring, making it a potential candidate for various chemical reactions, including nucleophilic additions and condensation reactions. The trifluoroethoxy substituent can enhance the compound's solubility in organic solvents and may also affect its biological activity. Additionally, the presence of fluorine atoms often imparts unique properties, such as increased lipophilicity and metabolic stability, which can be advantageous in pharmaceutical applications. Overall, this compound's structure suggests potential utility in synthetic organic chemistry and medicinal chemistry, particularly in the development of novel therapeutic agents.

6-(2,2,2-TRIFLUORO-ETHOXY)-PYRIDINE-3-CARBALDEHYDE

159981-19-8: 6-(2,2,2-Trifluoroethoxy)pyridine-3-carbaldehyde is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of the trifluoroethoxy group introduces significant electronegativity due to the three fluorine atoms, which can influence the compound's reactivity and polarity. This compound features an aldehyde functional group (-CHO) at the 3-position of the pyridine ring, making it a potential candidate for various chemical reactions, including nucleophilic additions and condensation reactions. The trifluoroethoxy substituent can enhance the compound's solubility in organic solvents and may also affect its biological activity. Additionally, the presence of fluorine atoms often imparts unique properties, such as increased lipophilicity and metabolic stability, which can be advantageous in pharmaceutical applications. Overall, this compound's structure suggests potential utility in synthetic organic chemistry and medicinal chemistry, particularly in the development of novel therapeutic agents.

CAS 159981-19-8

6-(2,2,2-TRIFLUORO-ETHOXY)-PYRIDINE-3-CARBALDEHYDE

3-Pyridinecarboxaldehyde, 6-(2,2,2-trifluoroethoxy)-

Ref: IN-DA001RK5

6-(2,2,2-Trifluoroethoxy)nicotinaldehyde

Ref: 54-PC100237

6-(2,2,2-Trifluoroethoxy)pyridine-3-carbaldehyde

Ref: 10-F210568