2-Chlorothiazolo[5,4-b]pyridine is a heterocyclic compound characterized by its unique bicyclic structure, which incorporates both thiazole and pyridine rings. This compound features a chlorine substituent at the 2-position of the thiazole ring, contributing to its chemical reactivity and potential biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of both nitrogen and sulfur atoms in its structure can influence its electronic properties, making it a candidate for various chemical reactions, including nucleophilic substitutions and cycloadditions. Additionally, compounds of this type are often investigated for their pharmacological properties, as they may exhibit antimicrobial, anti-inflammatory, or anticancer activities. The specific interactions and reactivity of 2-chlorothiazolo[5,4-b]pyridine can be influenced by the electronic effects of the chlorine atom and the overall molecular geometry. As with many heterocycles, its synthesis and functionalization are of interest in medicinal chemistry and materials science.

2-chlorothiazolo[5,4-b]pyridine

91524-96-8: 2-Chlorothiazolo[5,4-b]pyridine is a heterocyclic compound characterized by its unique bicyclic structure, which incorporates both thiazole and pyridine rings. This compound features a chlorine substituent at the 2-position of the thiazole ring, contributing to its chemical reactivity and potential biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of both nitrogen and sulfur atoms in its structure can influence its electronic properties, making it a candidate for various chemical reactions, including nucleophilic substitutions and cycloadditions. Additionally, compounds of this type are often investigated for their pharmacological properties, as they may exhibit antimicrobial, anti-inflammatory, or anticancer activities. The specific interactions and reactivity of 2-chlorothiazolo[5,4-b]pyridine can be influenced by the electronic effects of the chlorine atom and the overall molecular geometry. As with many heterocycles, its synthesis and functionalization are of interest in medicinal chemistry and materials science.

CAS 91524-96-8

2-chlorothiazolo[5,4-b]pyridine

2-CHLOROTHIAZOLO[5,4-B]PYRIDINE

Ref: IN-DA0069MP

2-Chlorothiazolo[5,4-b]pyridine

Ref: 54-OR94218

2-Chlorothiazolo[5,4-b]pyridine

Ref: 10-F220330