2-Bromo-4-nitropyridine is an organic compound characterized by the presence of both bromine and nitro functional groups attached to a pyridine ring. Its molecular formula is C5H4BrN3O2, indicating that it contains five carbon atoms, four hydrogen atoms, one bromine atom, three nitrogen atoms, and two oxygen atoms. This compound typically appears as a yellow to orange crystalline solid and is known for its moderate solubility in polar organic solvents. The presence of the bromine atom contributes to its reactivity, making it useful in various chemical synthesis applications, particularly in the development of pharmaceuticals and agrochemicals. The nitro group enhances its electrophilic properties, allowing it to participate in further chemical reactions, such as nucleophilic substitutions. Additionally, 2-Bromo-4-nitropyridine may exhibit biological activity, which can be of interest in medicinal chemistry. As with many halogenated compounds, appropriate safety measures should be taken when handling this substance due to potential toxicity and environmental concerns.

2-Bromo-4-nitropyridine

2-Bromo-4-nitropyridine is a molecule that contains a polarizability, hydrogen bond, and molecular electrostatic potential. It has been used to study the effects of solvent on the stability of molecules. X-ray data from 2-bromo-4-nitropyridine was collected at the Argonne National Laboratory. The molecular electrostatic potential was calculated using quantum chemistry calculations and vibrational spectroscopy data. The homoconjugation in 2-bromo-4-nitropyridine is due to its acetonitrile group and nitro group, which are both electron donating groups.
2-Bromo-4-nitropyridine has been synthesized using synthetic chemistry with dipole bonds cleaving during the reaction.

CAS 6945-67-1: 2-Bromo-4-nitropyridine

2-Bromo-4-nitropyridine

Ref: IN-DA003GOW

2-Bromo-4-nitropyridine

Ref: 3B-B3523

2-Bromo-4-nitropyridine

Ref: 3D-FB55521

2-Bromo-4-nitropyridine

Ref: 54-OR3139

2-Bromo-4-nitropyridine

Ref: 10-F067256