5-Bromo-N,3-dimethylpyridin-2-amine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a bromine atom at the 5-position and two methyl groups at the 3-position of the pyridine ring contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents due to the presence of the amino group, which can engage in hydrogen bonding. The amino group also makes it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the bromine substituent can serve as a leaving group in certain reactions, enhancing its utility in synthetic organic chemistry. The compound may also exhibit biological activity, making it of interest in pharmaceutical research. As with many nitrogen-containing heterocycles, it may participate in coordination chemistry, forming complexes with metal ions. Safety and handling precautions should be observed due to the potential reactivity of halogenated compounds.

5-bromo-N,3-diMethylpyridin-2-amine

245765-66-6: 5-Bromo-N,3-dimethylpyridin-2-amine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a bromine atom at the 5-position and two methyl groups at the 3-position of the pyridine ring contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents due to the presence of the amino group, which can engage in hydrogen bonding. The amino group also makes it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the bromine substituent can serve as a leaving group in certain reactions, enhancing its utility in synthetic organic chemistry. The compound may also exhibit biological activity, making it of interest in pharmaceutical research. As with many nitrogen-containing heterocycles, it may participate in coordination chemistry, forming complexes with metal ions. Safety and handling precautions should be observed due to the potential reactivity of halogenated compounds.

2-Pyridinamine, 5-bromo-N,3-dimethyl-

<p>5-Bromo-3-methyl-2-(methylamino)pyridine</p>

CAS 245765-66-6

5-bromo-N,3-diMethylpyridin-2-amine

2-Pyridinamine, 5-bromo-N,3-dimethyl-

Ref: IN-DA002OMP

5-Bromo-3-methyl-2-(methylamino)pyridine

Ref: 54-OR48105

5-Bromo-N,3-dimethylpyridin-2-amine

Ref: 10-F323864