3-Bromo-6-ethyl-5-methylisothiazolo[5,4-b]pyridine is a heterocyclic compound characterized by its unique bicyclic structure that incorporates both isothiazole and pyridine moieties. This compound features a bromine atom and ethyl and methyl substituents, which contribute to its chemical reactivity and physical properties. Typically, such compounds exhibit moderate to high solubility in organic solvents, while their solubility in water may vary depending on the substituents' nature and position. The presence of the isothiazole ring often imparts biological activity, making these compounds of interest in medicinal chemistry and drug development. Additionally, the bromine substituent can enhance the compound's reactivity in various chemical reactions, such as nucleophilic substitutions or coupling reactions. The compound's structure suggests potential applications in fields such as agrochemicals, pharmaceuticals, or materials science, where specific interactions with biological targets or materials are desired. As with many heterocycles, the stability and reactivity of 3-bromo-6-ethyl-5-methylisothiazolo[5,4-b]pyridine can be influenced by environmental factors such as pH and temperature.

3-bromo-6-ethyl-5-methylisothiazolo[5,4-b]pyridine

728885-92-5: 3-Bromo-6-ethyl-5-methylisothiazolo[5,4-b]pyridine is a heterocyclic compound characterized by its unique bicyclic structure that incorporates both isothiazole and pyridine moieties. This compound features a bromine atom and ethyl and methyl substituents, which contribute to its chemical reactivity and physical properties. Typically, such compounds exhibit moderate to high solubility in organic solvents, while their solubility in water may vary depending on the substituents' nature and position. The presence of the isothiazole ring often imparts biological activity, making these compounds of interest in medicinal chemistry and drug development. Additionally, the bromine substituent can enhance the compound's reactivity in various chemical reactions, such as nucleophilic substitutions or coupling reactions. The compound's structure suggests potential applications in fields such as agrochemicals, pharmaceuticals, or materials science, where specific interactions with biological targets or materials are desired. As with many heterocycles, the stability and reactivity of 3-bromo-6-ethyl-5-methylisothiazolo[5,4-b]pyridine can be influenced by environmental factors such as pH and temperature.

CAS 728885-92-5

3-bromo-6-ethyl-5-methylisothiazolo[5,4-b]pyridine

3-Bromo-6-ethyl-5-methylisothiazolo[5,4-b]pyridine

Ref: IN-DA005O12

3-bromo-6-ethyl-5-methylisothiazolo[5,4-b]pyridine

Ref: 10-F316176