5-Amino-2-chloro-4,6-dimethylpyridine-3-carbonitrile is a heterocyclic organic compound characterized by its pyridine ring, which contains various functional groups that contribute to its chemical properties. The presence of an amino group (-NH2) and a cyano group (-C≡N) indicates potential for reactivity, particularly in nucleophilic substitution reactions. The chlorine atom introduces electrophilic characteristics, while the dimethyl groups enhance the compound's hydrophobicity and steric bulk. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. The compound's reactivity can be influenced by the electronic effects of the substituents on the pyridine ring, making it a subject of interest in medicinal chemistry and material science. Safety data should be consulted for handling, as the presence of the cyano group can pose toxicity risks. Overall, 5-amino-2-chloro-4,6-dimethylpyridine-3-carbonitrile is a versatile compound with significant implications in various chemical applications.

5-amino-2-chloro-4,6-dimethylpyridine-3-carbonitrile

6972-36-7: 5-Amino-2-chloro-4,6-dimethylpyridine-3-carbonitrile is a heterocyclic organic compound characterized by its pyridine ring, which contains various functional groups that contribute to its chemical properties. The presence of an amino group (-NH2) and a cyano group (-C≡N) indicates potential for reactivity, particularly in nucleophilic substitution reactions. The chlorine atom introduces electrophilic characteristics, while the dimethyl groups enhance the compound's hydrophobicity and steric bulk. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. The compound's reactivity can be influenced by the electronic effects of the substituents on the pyridine ring, making it a subject of interest in medicinal chemistry and material science. Safety data should be consulted for handling, as the presence of the cyano group can pose toxicity risks. Overall, 5-amino-2-chloro-4,6-dimethylpyridine-3-carbonitrile is a versatile compound with significant implications in various chemical applications.

CAS 6972-36-7

5-amino-2-chloro-4,6-dimethylpyridine-3-carbonitrile

5-amino-2-chloro-4,6-dimethylnicotinonitrile

Ref: 10-F494983

5-Amino-2-chloro-4,6-dimethylpyridine-3-carbonitrile

Ref: 3D-GAA97236