3,5-Dibromo-4-ethylpyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with two bromine atoms at the 3 and 5 positions and an ethyl group at the 4 position. This compound typically appears as a colorless to light yellow liquid or solid, depending on its physical state at room temperature. It is known for its moderate to high reactivity due to the presence of the bromine substituents, which can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The ethyl group contributes to its hydrophobic character, influencing its solubility in organic solvents while being less soluble in water. 3,5-Dibromo-4-ethylpyridine may exhibit biological activity, making it of interest in pharmaceutical research and development. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Proper storage and handling protocols are essential to mitigate any potential hazards associated with this compound.

3,5-dibromo-4-ethylpyridine

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3,5-Dibromo-4-ethylpyridine

3,5-Dibromo-4-ethylpyridine is a pyridine derivative that is synthesized by the sequential metalation of 3,5-dibromopyridine with ethylmagnesium bromide. This compound undergoes lithiation with n-butyllithium followed by electrophilic substitution of the bromide group with an electron-rich aromatic ring. The resulting compound has been shown to be an effective electrophile in organic synthesis.

CAS 125419-80-9: 3,5-dibromo-4-ethylpyridine

3,5-Dibromo-4-ethylpyridine

Ref: IN-DA009D4T

3,5-Dibromo-4-ethylpyridine

Ref: 10-F629666

3,5-Dibromo-4-ethylpyridine

Ref: 3D-FD55857