2-(1H-Pyrrol-1-yl)thiazole is an organic compound characterized by the presence of both a pyrrole and a thiazole ring in its structure. The pyrrole ring contributes to its aromatic properties, while the thiazole ring introduces heteroatoms, specifically sulfur and nitrogen, which can influence its reactivity and biological activity. This compound typically exhibits a range of physical properties, including moderate solubility in polar solvents due to the presence of nitrogen and sulfur, which can engage in hydrogen bonding. It may also display interesting electronic properties due to the conjugated system formed by the fused rings. 2-(1H-Pyrrol-1-yl)thiazole has garnered attention in medicinal chemistry for its potential biological activities, including antimicrobial and anticancer properties, making it a subject of interest for drug development. Its synthesis often involves multi-step organic reactions, and its stability can vary based on environmental conditions. As with many heterocyclic compounds, its reactivity can be influenced by substituents on the rings, which can modulate its pharmacological profile.

2-(1H-Pyrrol-1-yl)thiazole

50966-77-3: 2-(1H-Pyrrol-1-yl)thiazole is an organic compound characterized by the presence of both a pyrrole and a thiazole ring in its structure. The pyrrole ring contributes to its aromatic properties, while the thiazole ring introduces heteroatoms, specifically sulfur and nitrogen, which can influence its reactivity and biological activity. This compound typically exhibits a range of physical properties, including moderate solubility in polar solvents due to the presence of nitrogen and sulfur, which can engage in hydrogen bonding. It may also display interesting electronic properties due to the conjugated system formed by the fused rings. 2-(1H-Pyrrol-1-yl)thiazole has garnered attention in medicinal chemistry for its potential biological activities, including antimicrobial and anticancer properties, making it a subject of interest for drug development. Its synthesis often involves multi-step organic reactions, and its stability can vary based on environmental conditions. As with many heterocyclic compounds, its reactivity can be influenced by substituents on the rings, which can modulate its pharmacological profile.

CAS 50966-77-3

2-(1H-Pyrrol-1-yl)thiazole

2-(1H-Pyrrol-1-yl)-1,3-thiazole

Ref: 54-OR32248