6-Fluoro-2-methyl-3-(methylthio)pyridine is a heterocyclic organic compound characterized by its pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. The presence of a fluorine atom at the 6-position and a methylthio group at the 3-position contributes to its unique chemical properties. This compound typically exhibits moderate polarity due to the electronegative fluorine atom and the sulfur atom in the methylthio group, influencing its solubility in various solvents. The methyl group at the 2-position enhances its hydrophobic character. As a pyridine derivative, it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Its structural features suggest potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. The compound's reactivity and stability can be influenced by the substituents on the pyridine ring, making it a subject of interest in medicinal chemistry and material science. Safety and handling precautions should be observed due to the potential toxicity associated with sulfur-containing compounds.

6-fluoro-2-methyl-3-(methylthio)pyridine

1204336-74-2: 6-Fluoro-2-methyl-3-(methylthio)pyridine is a heterocyclic organic compound characterized by its pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. The presence of a fluorine atom at the 6-position and a methylthio group at the 3-position contributes to its unique chemical properties. This compound typically exhibits moderate polarity due to the electronegative fluorine atom and the sulfur atom in the methylthio group, influencing its solubility in various solvents. The methyl group at the 2-position enhances its hydrophobic character. As a pyridine derivative, it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Its structural features suggest potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. The compound's reactivity and stability can be influenced by the substituents on the pyridine ring, making it a subject of interest in medicinal chemistry and material science. Safety and handling precautions should be observed due to the potential toxicity associated with sulfur-containing compounds.

CAS 1204336-74-2

6-fluoro-2-methyl-3-(methylthio)pyridine

6-Fluoro-2-methyl-3-(methylthio)pyridine

Ref: IN-DA01DNNQ

6-Fluoro-2-methyl-3-(methylthio)pyridine

Ref: 10-F632497