4-Chloro-2,6-diaminopyridine is an organic compound with the molecular formula C5H7ClN4. It features a pyridine ring substituted with two amino groups at the 2 and 6 positions and a chlorine atom at the 4 position. This compound is typically a solid at room temperature and is known for its potential applications in pharmaceuticals and agrochemicals. It exhibits basic properties due to the presence of amino groups, which can participate in hydrogen bonding and protonation reactions. The chlorine substituent can influence the compound's reactivity and solubility in various solvents. Additionally, 4-Chloro-2,6-diaminopyridine may be involved in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in organic synthesis. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled. Proper storage conditions are also essential to maintain its stability and prevent degradation.

4-Chloro-2,6-diaminopyridine

6309-00-8: 4-Chloro-2,6-diaminopyridine is an organic compound with the molecular formula C5H7ClN4. It features a pyridine ring substituted with two amino groups at the 2 and 6 positions and a chlorine atom at the 4 position. This compound is typically a solid at room temperature and is known for its potential applications in pharmaceuticals and agrochemicals. It exhibits basic properties due to the presence of amino groups, which can participate in hydrogen bonding and protonation reactions. The chlorine substituent can influence the compound's reactivity and solubility in various solvents. Additionally, 4-Chloro-2,6-diaminopyridine may be involved in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in organic synthesis. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled. Proper storage conditions are also essential to maintain its stability and prevent degradation.

2,6-DIAMINO-4-CHLOROPYRIDINE

<p>4-Chloropyridine-2,6-diamine is a compound that contains nitrogen and carbon. It has been synthesized experimentally and the crystal structure has been determined by X-ray crystallography. This substance belongs to the class of heterocycles and it is a hydrogen bond acceptor. The crystal structure of 4-chloropyridine-2,6-diamine has been rationalized using experimental data. The electron density maps show that there are six moles of naphthalene for every mole of 4-chloropyridine-2,6-diamine in the crystal lattice. <br>4-Chloropyridine-2,6-diamine is an enthalpy donor because it donates its electrons to other substances. It also accepts hydrogen bonds from other substances. This substance can form supramolecular frameworks with pyridine and benzene molecules, which stabilizes the molecule's structure through coval</p>

CAS 6309-00-8

4-Chloro-2,6-diaminopyridine

2,6-DIAMINO-4-CHLOROPYRIDINE

Ref: IN-DA00EAHW

4-chloropyridine-2,6-diamine

Ref: 3D-GAA30900