3-Methyl-2,6-pyridinediamine, also known by its CAS number 51566-22-4, is an organic compound characterized by its pyridine ring structure, which is substituted with two amino groups and a methyl group. This compound typically appears as a solid at room temperature and is soluble in polar solvents due to the presence of amino groups that can engage in hydrogen bonding. The amino groups contribute to its basicity, making it reactive in various chemical reactions, including nucleophilic substitutions and coupling reactions. 3-Methyl-2,6-pyridinediamine is often utilized in the synthesis of dyes, pharmaceuticals, and agrochemicals, owing to its ability to act as a building block in organic synthesis. Additionally, it may exhibit biological activity, which can be of interest in medicinal chemistry. Safety data should be consulted, as with any chemical, to understand its handling, storage, and potential hazards. Overall, this compound is significant in both industrial and research applications due to its versatile reactivity and structural features.

3-Methyl-2,6-pyridinediamine

51566-22-4: 3-Methyl-2,6-pyridinediamine, also known by its CAS number 51566-22-4, is an organic compound characterized by its pyridine ring structure, which is substituted with two amino groups and a methyl group. This compound typically appears as a solid at room temperature and is soluble in polar solvents due to the presence of amino groups that can engage in hydrogen bonding. The amino groups contribute to its basicity, making it reactive in various chemical reactions, including nucleophilic substitutions and coupling reactions. 3-Methyl-2,6-pyridinediamine is often utilized in the synthesis of dyes, pharmaceuticals, and agrochemicals, owing to its ability to act as a building block in organic synthesis. Additionally, it may exhibit biological activity, which can be of interest in medicinal chemistry. Safety data should be consulted, as with any chemical, to understand its handling, storage, and potential hazards. Overall, this compound is significant in both industrial and research applications due to its versatile reactivity and structural features.

CAS 51566-22-4

3-Methyl-2,6-pyridinediamine

3-Methylpyridine-2,6-diamine

Ref: IN-DA00DJ4A

3-Methylpyridine-2,6-diamine

Ref: 54-OR81531

3-Methylpyridine-2,6-diamine

Ref: 10-F225632