CAS 33631-09-3

4-methoxypyridin-3-amine

Description:

4-Methoxypyridin-3-amine, with the CAS number 33631-09-3, is an organic compound characterized by a pyridine ring substituted with a methoxy group and an amino group. The methoxy group (-OCH3) is located at the 4-position, while the amino group (-NH2) is at the 3-position of the pyridine ring. This compound is typically a solid at room temperature and is soluble in polar solvents due to the presence of the amino group, which can engage in hydrogen bonding. It exhibits basic properties due to the amino group, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The presence of both electron-donating (methoxy) and electron-withdrawing (pyridine nitrogen) groups can influence its reactivity and interaction with other molecules. 4-Methoxypyridin-3-amine is of interest in medicinal chemistry and may serve as a building block for the synthesis of pharmaceuticals or agrochemicals. Its specific applications and biological activities would depend on further research and exploration within the field.

Formula: C₆H₈N₂O

InChI: InChI=1/C6H8N2O/c1-9-6-2-3-8-4-5(6)7/h2-4H,7H2,1H3

SMILES: COc1ccncc1N

Synonyms:

• 3-Amino-4-methoxypyridine
• 3-Pyridinamine, 4-methoxy-

3-Amino-4-methoxypyridine

CAS: 33631-09-3

Formula: C₆H₈N₂O

Purity: 97%

Color and Shape: Solid

Molecular weight: 124.1405

Ref: IN-DA00BYHX

3-Amino-4-methoxypyridine

CAS: 33631-09-3

3-Amino-4-methoxypyridine

Formula: C₆H₈N₂O

Purity: 97%

Color and Shape: brown to red solid

Molecular weight: 124.14g/mol

Ref: 54-OR42156

3-Amino-4-methoxypyridine

CAS: 33631-09-3

Formula: C₆H₈N₂O

Purity: 95%

Color and Shape: Solid

Molecular weight: 124.143

Ref: 10-F076885

3-Amino-4-methoxypyridine

CAS: 33631-09-3

3-Amino-4-methoxypyridine is a molecule that has been shown to have anesthetic activity. It has been shown to inhibit the uptake of glycogen by glioblastoma cells and decrease the rate of glycogen synthesis in these cells. 3-Amino-4-methoxypyridine also inhibits the production of ATP in cardiac muscle cells, which may be due to its ability to inhibit glycogen synthase kinase-3 (GSK3) and glycogen synthase. This drug also inhibits cancer cell growth by inhibiting protein synthesis, as well as inflammatory disease progression by inhibiting NFκB activation and cytokine production. 3-Amino-4-methoxypyridine can be synthesized from aminopyridines such as isonicotinic acid or nicotinic acid, which are oxidized with hydrogen peroxide and sodium nitrite in the presence of a base catalyst.

Formula: C₆H₈N₂O

Purity: Min. 95%

Molecular weight: 124.14 g/mol

Ref: 3D-FA46267