5-Bromo-N3-methyl-2,3-pyridinediamine, with the CAS number 166047-15-0, is a chemical compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features a bromine substituent at the 5-position and a methyl group at the N3 position of the pyridine ring, along with two amino groups (–NH2) at the 2 and 3 positions. The presence of these functional groups contributes to its potential reactivity and solubility in various solvents. Typically, compounds like this may exhibit biological activity, making them of interest in medicinal chemistry and drug development. The bromine atom can enhance the compound's lipophilicity and may influence its interaction with biological targets. Additionally, the amino groups can participate in hydrogen bonding, affecting the compound's physical properties and reactivity. Overall, 5-Bromo-N3-methyl-2,3-pyridinediamine is a versatile compound with potential applications in various fields, including pharmaceuticals and agrochemicals.

5-Bromo-N3-methyl-2,3-pyridinediamine

166047-15-0: 5-Bromo-N3-methyl-2,3-pyridinediamine, 5-Bromo-N3-methylpyridine-2,3-diamine, 2,3-Pyridinediamine, 5-bromo-N3-methyl-

2,3-Pyridinediamine, 5-bromo-N3-methyl-

5-Bromo-N3-methylpyridine-2,3-diamine

5-Bromo-N3-methylpyridine-2,3-diamine is a halogenated pyridine derivative that is the product of bromination and chlorination reactions. 5-Bromo-N3-methylpyridine-2,3-diamine can be used as an intermediate in the production of other chemicals such as dyes and pharmaceuticals. The pathways for the synthesis of 5-bromo-N3 methylpyridine 2,3 diamine are shown below.

CAS 166047-15-0: 5-Bromo-N3-methyl-2,3-pyridinediamine

2,3-Pyridinediamine, 5-bromo-N3-methyl-

Ref: IN-DA001WGH

5-Bromo-N3-methylpyridine-2,3-diamine

Ref: 54-OR83605

5-Bromo-N3-methylpyridine-2,3-diamine

Ref: 10-F634247

5-Bromo-N3-methylpyridine-2,3-diamine

Ref: 3D-RGA04715