2,6-Dichloro-3-(methoxymethyl)pyridine is an organic compound characterized by its pyridine ring, which is substituted at the 2 and 6 positions with chlorine atoms and at the 3 position with a methoxymethyl group. This structure imparts specific chemical properties, including increased lipophilicity due to the presence of the methoxymethyl group, which can enhance its solubility in organic solvents. The dichloro substitutions contribute to its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The compound may exhibit biological activity, which can be explored in pharmaceutical applications, particularly in the development of agrochemicals or medicinal compounds. Its molecular structure suggests potential interactions with biological targets, although specific biological activity would require empirical investigation. Safety data should be reviewed, as halogenated compounds can pose environmental and health risks. Overall, 2,6-Dichloro-3-(methoxymethyl)pyridine is a versatile compound with applications in synthetic chemistry and potential implications in various fields.

2,6-Dichloro-3-(methoxymethyl)pyridine

1330763-31-9: 2,6-Dichloro-3-methoxymethylpyridine, Pyridine, 2,6-dichloro-3-(methoxymethyl)-, 2,6-Dichloro-3-(methoxymethyl)pyridine

CAS 1330763-31-9: 2,6-Dichloro-3-(methoxymethyl)pyridine

2,6-Dichloro-3-Methoxymethyl-Pyridine

Ref: IN-DA00HSR1

2,6-DICHLORO-3-METHOXYMETHYL-PYRIDINE

Ref: 10-F505443

2,6-dichloro-3-(methoxymethyl)pyridine

Ref: 3D-FDC76331