2,3-Dichloro-4-pyridinamine, with the CAS number 184416-83-9, is an organic compound characterized by its pyridine ring substituted with two chlorine atoms and an amino group. 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 in various solvents. The amino group contributes to its basicity and potential for forming hydrogen bonds, which can affect its interactions with biological targets. Additionally, the compound's structure suggests it may participate in electrophilic aromatic substitution reactions, making it a versatile intermediate in organic synthesis. Safety data indicates that, like many chlorinated compounds, it should be handled with care due to potential toxicity and environmental concerns. Overall, 2,3-Dichloro-4-pyridinamine is a significant compound in chemical research, particularly in the development of new materials and pharmaceuticals.

2,3-Dichloro-4-pyridinamine

184416-83-9: 2,3-Dichloro-4-pyridinamine, 4-Amino-2,3-dichloropyridine, 4-Pyridinamine, 2,3-dichloro-, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 

CAS 184416-83-9: 2,3-Dichloro-4-pyridinamine

2,3-Dichloropyridin-4-amine

Ref: 10-F325032

4-Amino-2,3-dichloropyridine

Ref: 3D-JHA41683

4-Amino-2,3-dichloropyridine

Ref: 54-OR303762

4-Pyridinamine,2,3-dichloro-(9CI)

Ref: IN-DA00AKIC