3-[(4-Chlorophenyl)sulfanyl]-5-(trifluoromethyl)pyridine-2-carbaldehyde is an organic compound characterized by its complex structure, which includes a pyridine ring substituted with a trifluoromethyl group and a chlorophenyl sulfanyl group. The presence of the trifluoromethyl group contributes to its unique electronic properties, enhancing its reactivity and potential applications in medicinal chemistry and agrochemicals. The aldehyde functional group at the pyridine's 2-position makes it a versatile intermediate for further chemical transformations, allowing for the synthesis of various derivatives. The chlorophenyl sulfanyl moiety adds to its potential biological activity, as sulfur-containing compounds often exhibit interesting pharmacological properties. This compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its chemical behavior can be influenced by the electron-withdrawing trifluoromethyl group and the electron-donating characteristics of the sulfanyl group, making it a subject of interest in research focused on developing new materials or pharmaceuticals. Safety data should be consulted for handling, as with all chemical substances.

3-[(4-chlorophenyl)sulfanyl]-5-(trifluoromethyl)pyridine-2-carbaldehyde

264924-39-2: 3-[(4-Chlorophenyl)sulfanyl]-5-(trifluoromethyl)pyridine-2-carbaldehyde is an organic compound characterized by its complex structure, which includes a pyridine ring substituted with a trifluoromethyl group and a chlorophenyl sulfanyl group. The presence of the trifluoromethyl group contributes to its unique electronic properties, enhancing its reactivity and potential applications in medicinal chemistry and agrochemicals. The aldehyde functional group at the pyridine's 2-position makes it a versatile intermediate for further chemical transformations, allowing for the synthesis of various derivatives. The chlorophenyl sulfanyl moiety adds to its potential biological activity, as sulfur-containing compounds often exhibit interesting pharmacological properties. This compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its chemical behavior can be influenced by the electron-withdrawing trifluoromethyl group and the electron-donating characteristics of the sulfanyl group, making it a subject of interest in research focused on developing new materials or pharmaceuticals. Safety data should be consulted for handling, as with all chemical substances.

CAS 264924-39-2

3-[(4-chlorophenyl)sulfanyl]-5-(trifluoromethyl)pyridine-2-carbaldehyde

2-Pyridinecarboxaldehyde, 3-[(4-chlorophenyl)thio]-5-(trifluoromethyl)-

Ref: IN-DA002TG7

3-[(4-chlorophenyl)thio]-5-(trifluoromethyl)pyridine-2-carboxaldehyde

Ref: 54-PC32624