2,3,6-Tribromopyridine is a halogenated aromatic compound characterized by the presence of three bromine atoms attached to a pyridine ring at the 2, 3, and 6 positions. Its molecular formula is C5H3Br3N, indicating a relatively low molecular weight. This compound typically appears as a colorless to pale yellow solid and is known for its distinctive aromatic odor. 2,3,6-Tribromopyridine is soluble in organic solvents such as acetone and chloroform but has limited solubility in water due to its hydrophobic nature. The presence of bromine atoms enhances its reactivity, making it useful in various chemical syntheses, particularly in the development of pharmaceuticals and agrochemicals. Additionally, it exhibits biological activity, which can be leveraged in medicinal chemistry. Safety precautions are necessary when handling this compound, as brominated compounds can pose environmental and health risks. Overall, 2,3,6-Tribromopyridine is a significant compound in organic synthesis and research applications.

2,3,6-Tribromopyridine

2402-92-8: Pyridine, 2,3,6-tribromo-, 2,3,6-Tribromopyridine

2,3,6-Tribromopyridine is a reactive chemical compound with the formula CHBrCl. It reacts with nucleophiles to form products that are useful in organic synthesis. The compound has been used as a biomolecule in cross-coupling reactions and is able to react with amines, n-oxides and alkoxides. 2,3,6-Tribromopyridine is also able to undergo halogenation reactions and can be protonated by phosphorus pentachloride to form an electrophilic species that can react with piperidine or methylamine. Cross-coupling reactions between 2,3,6-Tribromopyridine and alkenes have been shown experimentally. The reaction product of this coupling isomerizes to give 1H-benzotriazole (1).

CAS 2402-92-8: 2,3,6-Tribromopyridine

2,3,6-Tribromopyridine

Ref: 54-OR94383

2,3,6-Tribromopyridine

Ref: 3D-CAA40292

2,3,6-Tribromopyridine

Ref: IN-DA00BH0A

2,3,6-Tribromopyridine

Ref: 10-F217946