3-Bromo-4-trifluoromethylpyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with a bromine atom at the 3-position and a trifluoromethyl group at the 4-position. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is known for its aromatic properties and is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals due to its unique electronic and steric properties imparted by the bromine and trifluoromethyl groups. The presence of the trifluoromethyl group enhances lipophilicity and can influence the compound's reactivity and biological activity. Additionally, 3-Bromo-4-trifluoromethylpyridine may exhibit moderate to high toxicity, necessitating careful handling and appropriate safety measures during its use in laboratory or industrial settings. Its chemical behavior can be influenced by the electron-withdrawing nature of the trifluoromethyl group, making it a valuable intermediate in various chemical reactions.

3-Bromo-4-trifluoromethylpyridine

936841-70-2: 3-Bromo-4-(trifluoromethyl)pyridine

3-Bromo-4-(trifluoromethyl)pyridine

3-bromo-4-(trifluoromethyl)pyridine is a n-oxide of an amination reaction. It belongs to the group of intramolecular enamines, and can be synthesized from pyridine. 3-bromo-4-(trifluoromethyl)pyridine reacts with nitrous acid to form an enamine, which undergoes hydrolysis to produce 3-nitrosobenzene. This intermediate reacts with ammonia to give an imine, which then undergoes hydrogenation to form the final product.

CAS 936841-70-2: 3-Bromo-4-trifluoromethylpyridine

3-Bromo-4-(trifluoromethyl)pyridine

Ref: 10-F038154

3-bromo-4-(trifluoromethyl)pyridine

Ref: 3D-FB105692

3-Bromo-4-trifluoromethylpyridine

Ref: IN-DA00GRC9

3-Bromo-4-(trifluoromethyl)pyridine

Ref: 54-PC7718