5-Chloro-3-methylpyridin-2-amine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The compound features a chlorine atom at the 5-position and a methyl group at the 3-position of the pyridine ring, along with an amino group (-NH2) at the 2-position. This structure contributes to its unique chemical properties, including its potential as a building block in pharmaceuticals and agrochemicals. The presence of the amino group makes it a basic compound, capable of forming salts with acids. Additionally, the chlorine substituent can influence the compound's reactivity and solubility in various solvents. 5-Chloro-3-methylpyridin-2-amine may exhibit biological activity, making it of interest in medicinal chemistry. Its CAS number, 20712-16-7, is a unique identifier that facilitates its identification in chemical databases and literature. Overall, this compound's characteristics make it valuable for further research and application in various chemical fields.

5-chloro-3-methylpyridin-2-amine

20712-16-7: 2-Amino-5-chloro-3-methylpyridine, 2-Pyridinamine, 5-chloro-3-methyl-, 5-Chloro-3-methyl-2-pyridinamine, Nsc508755, 2-Amino-5-Chloro-3-Picoline

2-Pyridinamine, 5-chloro-3-methyl-

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CAS 20712-16-7: 5-chloro-3-methylpyridin-2-amine

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2-Amino-5-chloro-3-methylpyridine

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