4,6-Dichloro-2,3-pyridinediamine, with the CAS number 24484-99-9, is an organic compound characterized by its pyridine ring structure, which is substituted at the 2 and 3 positions with amino groups and at the 4 and 6 positions with chlorine atoms. This compound typically appears as a solid and is known for its potential applications in pharmaceuticals and agrochemicals due to its biological activity. The presence of chlorine atoms enhances its reactivity and may influence its solubility and stability in various solvents. As a diamine, it can participate in various chemical reactions, including those involving nucleophilic substitution and condensation. Safety data indicates that, like many chlorinated compounds, it should be handled with care, as it may pose health risks upon exposure. Its synthesis and use are subject to regulatory scrutiny, particularly concerning environmental impact and safety. Overall, 4,6-Dichloro-2,3-pyridinediamine is a compound of interest in both research and industrial applications.

4,6-Dichloro-2,3-pyridinediamine

24484-99-9: 2,3-Pyridinediamine, 4,6-dichloro-, 2,3-Diamino-4,6-dichloropyridine, 4,6-Dichloro-2,3-pyridinediamine, Pyridine, 2,3-diamino-4,6-dichloro-

CAS 24484-99-9: 4,6-Dichloro-2,3-pyridinediamine

4,6-Dichloropyridine-2,3-diamine

Ref: 3D-ZAA48499

2,3-Pyridinediamine, 4,6-dichloro-

Ref: IN-DA002OAI

4,6-Dichloropyridine-2,3-diamine

Ref: 10-F519590

4,6-Dichloropyridine-2,3-diamine

Ref: 54-OR76959