2-Amino-3-methoxypyridine is an organic compound characterized by a pyridine ring substituted with an amino group and a methoxy group. Its molecular structure features a six-membered aromatic ring containing one nitrogen atom, which contributes to its basicity and potential reactivity. The amino group (-NH2) is a strong electron-donating group, enhancing the compound's nucleophilicity, while the methoxy group (-OCH3) is an electron-donating substituent that can influence the compound's solubility and reactivity. This compound is typically a colorless to pale yellow liquid or solid, depending on its form, and is soluble in polar solvents. It is often used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. The presence of both amino and methoxy groups allows for diverse chemical reactions, including alkylation, acylation, and coupling reactions, making it a valuable building block in synthetic chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.

2-Amino-3-methoxypyridine

10201-71-5: 2-Pyridinamine, 3-Methoxy-, 3-Methoxypyridin-2-amine

2-Amino-3-methoxypyridine is a reactive compound that has been shown to react with hydrogen gas, water, and acids. It can be used as a ligand for inorganic ions such as copper (Cu), nickel (Ni), and cobalt (Co). 2-Amino-3-methoxypyridine is also reactive with nucleophiles such as thiols, amines, and alcohols. The reactive site of the molecule is the pyridinium nitrogen atom. This compound reacts with protonated water molecules to form an acid complex (RCOOH) and hydrogen bond formation.

CAS 10201-71-5: 2-Amino-3-methoxypyridine

2-Amino-3-methoxypyridine

Ref: 3D-FA54411

2-Amino-3-methoxypyridine

Ref: 10-F050813

2-Pyridinamine, 3-methoxy-

Ref: IN-DA0006BM

2-Amino-3-methoxypyridine

Ref: 54-OR8879