4,7-Dimethoxy-1H-pyrrolo[2,3-c]pyridine is a heterocyclic organic compound characterized by its pyrrolo[2,3-c]pyridine core structure, which features a fused bicyclic system. The presence of two methoxy groups at the 4 and 7 positions contributes to its chemical properties, influencing its solubility, reactivity, and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its molecular structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry and drug development. The methoxy substituents can enhance lipophilicity, potentially improving membrane permeability. Additionally, the compound may exhibit fluorescence properties, which can be useful in various analytical applications. As with many heterocycles, it may participate in diverse chemical reactions, including electrophilic substitutions and nucleophilic attacks, depending on the reaction conditions. Overall, 4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridine is a compound of interest for further research in both synthetic and medicinal chemistry contexts.

4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridine

452296-79-6: 4,7-Dimethoxy-1H-pyrrolo[2,3-c]pyridine is a heterocyclic organic compound characterized by its pyrrolo[2,3-c]pyridine core structure, which features a fused bicyclic system. The presence of two methoxy groups at the 4 and 7 positions contributes to its chemical properties, influencing its solubility, reactivity, and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its molecular structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry and drug development. The methoxy substituents can enhance lipophilicity, potentially improving membrane permeability. Additionally, the compound may exhibit fluorescence properties, which can be useful in various analytical applications. As with many heterocycles, it may participate in diverse chemical reactions, including electrophilic substitutions and nucleophilic attacks, depending on the reaction conditions. Overall, 4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridine is a compound of interest for further research in both synthetic and medicinal chemistry contexts.

CAS 452296-79-6

4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridine

4,7-Dimethoxy-1H-pyrrolo[2,3-c]pyridine

Ref: IN-DA00DM2A