5-Chloropyridine-3,4-diamine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of two amino groups (-NH2) at the 3 and 4 positions of the pyridine ring, along with a chlorine substituent at the 5 position, contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the amino groups, which can engage in hydrogen bonding. Its structure allows for potential reactivity in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it of interest in pharmaceutical and agrochemical research. Additionally, the chlorine atom can influence the electronic properties of the molecule, potentially affecting its biological activity. Safety data should be consulted for handling, as with many nitrogen-containing compounds, it may pose health risks if not managed properly. Overall, 5-chloropyridine-3,4-diamine is a versatile compound with applications in synthetic organic chemistry.

5-chloropyridine-3,4-diamine

929074-42-0: 5-Chloropyridine-3,4-diamine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of two amino groups (-NH2) at the 3 and 4 positions of the pyridine ring, along with a chlorine substituent at the 5 position, contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the amino groups, which can engage in hydrogen bonding. Its structure allows for potential reactivity in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it of interest in pharmaceutical and agrochemical research. Additionally, the chlorine atom can influence the electronic properties of the molecule, potentially affecting its biological activity. Safety data should be consulted for handling, as with many nitrogen-containing compounds, it may pose health risks if not managed properly. Overall, 5-chloropyridine-3,4-diamine is a versatile compound with applications in synthetic organic chemistry.

CAS 929074-42-0

5-chloropyridine-3,4-diamine

5-Chloro-3,4-diaminopyridine

Ref: IN-DA00GV02

5-Chloro-3,4-diaminopyridine

Ref: 54-OR345157

5-Chloropyridine-3,4-diamine

Ref: 10-F214753