2,6-Dibromo-4-nitropyridine is a heterocyclic organic compound characterized by its pyridine ring substituted with two bromine atoms at the 2 and 6 positions and a nitro group at the 4 position. This compound typically appears as a solid and is known for its pale yellow to brown color. It is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and dichloromethane, but has limited solubility in water. The presence of both bromine and nitro groups contributes to its reactivity, making it useful in various chemical syntheses, particularly in the development of pharmaceuticals and agrochemicals. The compound exhibits notable electronic properties due to the electron-withdrawing nature of the nitro group, which can influence its behavior in chemical reactions. Additionally, 2,6-Dibromo-4-nitropyridine may have applications in materials science and as an intermediate in organic synthesis. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.

2,6-Dibromo-4-nitropyridine

175422-04-5: 2,6-Dibromo-4-Nitropyridine, Pyridine, 2,6-dibromo-4-nitro-

2,6-Dibromo-4-nitro-pyridine

2,6-Dibromo-4-nitropyridine is an unsymmetrical compound with a bicyclic structure. The nitro group on the 6 position of the pyridine ring is chemically different than the two nitro groups on the 4 position, which are ortho to each other. This difference in reactivity can be exploited in a regioselective synthesis. The crystal structures of 2,6-dibromo-4-nitropyridine and its derivatives have been determined by x-ray diffraction analysis. A coupling reaction has been carried out to synthesize 2,6-dibromo-4-(2′,3′-dimethoxybenzoyl)pyridine from 2,6-dibromopyridine and 2,3'-dimethoxybenzoic acid.

CAS 175422-04-5: 2,6-Dibromo-4-nitropyridine

2,6-Dibromo-4-nitro-pyridine

Ref: 10-F041114

2,6-Dibromo-4-nitropyridine

Ref: 3D-FD142976

Pyridine, 2,6-dibromo-4-nitro-

Ref: IN-DA0020Z2

2,6-Dibromo-4-nitro-pyridine

Ref: 54-OR313044