3-Chloro-2-(trifluoromethyl)pyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with a chlorine atom and a trifluoromethyl group. The presence of the chlorine atom at the 3-position and the trifluoromethyl group at the 2-position significantly influences its chemical properties, including its reactivity and polarity. This compound is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It is known for its applications in pharmaceuticals and agrochemicals, often serving as an intermediate in the synthesis of more complex molecules. The trifluoromethyl group enhances the lipophilicity and metabolic stability of the compound, making it valuable in medicinal chemistry. Additionally, 3-chloro-2-(trifluoromethyl)pyridine exhibits moderate to high toxicity, necessitating careful handling and storage. Its unique structural features contribute to its role in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a compound of interest in both industrial and research settings.

3-chloro-2-(trifluoromethyl)pyridine

749875-32-9: 3-Chloro-2-(trifluoromethyl)pyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with a chlorine atom and a trifluoromethyl group. The presence of the chlorine atom at the 3-position and the trifluoromethyl group at the 2-position significantly influences its chemical properties, including its reactivity and polarity. This compound is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It is known for its applications in pharmaceuticals and agrochemicals, often serving as an intermediate in the synthesis of more complex molecules. The trifluoromethyl group enhances the lipophilicity and metabolic stability of the compound, making it valuable in medicinal chemistry. Additionally, 3-chloro-2-(trifluoromethyl)pyridine exhibits moderate to high toxicity, necessitating careful handling and storage. Its unique structural features contribute to its role in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a compound of interest in both industrial and research settings.

3-Chloro-2-(trifluoromethyl)-pyridine

<p>3-Chloro-2-(trifluoromethyl)pyridine</p>

CAS 749875-32-9

3-chloro-2-(trifluoromethyl)pyridine

3-Chloro-2-(trifluoromethyl)-pyridine

Ref: IN-DA0057GH

3-Chloro-2-(trifluoromethyl)pyridine

Ref: 54-PC520592

3-Chloro-2-(trifluoromethyl)pyridine

Ref: 10-F038152

3-Chloro-2-(trifluoromethyl)pyridine

Ref: TR-C421735