5-(Trifluoromethyl)pyridine-3-carbonitrile is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a trifluoromethyl group (-CF3) at the 5-position of the pyridine ring significantly influences its chemical properties, enhancing its lipophilicity and potentially its reactivity. The carbonitrile functional group (-C≡N) at the 3-position introduces a polar and reactive site, making the compound useful in various synthetic applications, including as an intermediate in the production of pharmaceuticals and agrochemicals. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its unique electronic properties, derived from the electron-withdrawing trifluoromethyl group, can affect its behavior in chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions. Safety data should be consulted for handling, as compounds with trifluoromethyl groups can exhibit toxicity and environmental persistence.

5-(trifluoromethyl)pyridine-3-carbonitrile

951624-83-2: 5-(Trifluoromethyl)pyridine-3-carbonitrile is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a trifluoromethyl group (-CF3) at the 5-position of the pyridine ring significantly influences its chemical properties, enhancing its lipophilicity and potentially its reactivity. The carbonitrile functional group (-C≡N) at the 3-position introduces a polar and reactive site, making the compound useful in various synthetic applications, including as an intermediate in the production of pharmaceuticals and agrochemicals. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its unique electronic properties, derived from the electron-withdrawing trifluoromethyl group, can affect its behavior in chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions. Safety data should be consulted for handling, as compounds with trifluoromethyl groups can exhibit toxicity and environmental persistence.

5-(Trifluoromethyl)nicotinonitrile

<p>5-(Trifluoromethyl)nicotinonitrile</p>

CAS 951624-83-2

5-(trifluoromethyl)pyridine-3-carbonitrile

5-(Trifluoromethyl)nicotinonitrile

Ref: IN-DA003M88

5-(Trifluoromethyl)nicotinonitrile

Ref: 54-PC520548

5-(Trifluoromethyl)nicotinonitrile

Ref: 10-F411964