4-Bromo-1H-isoindole-1,3(2H)-dione, with the CAS number 70478-63-6, is a chemical compound characterized by its isoindole structure, which features a fused benzene and pyrrole ring system. The presence of a bromine atom at the 4-position contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. This compound typically exhibits a solid state at room temperature and is known for its stability under standard conditions. It is often utilized in research for its potential biological activities, including antimicrobial and anticancer properties. The dione functional groups in its structure suggest the ability to participate in various chemical reactions, such as nucleophilic additions and cycloadditions. Its solubility may vary depending on the solvent, but it is generally more soluble in organic solvents than in water. As with many brominated compounds, safety precautions should be taken due to potential toxicity and environmental impact. Overall, 4-bromo-1H-isoindole-1,3(2H)-dione is a compound of interest in both synthetic and medicinal chemistry.

4-bromo-1H-isoindole-1,3(2H)-dione

70478-63-6: 4-Bromo-1H-isoindole-1,3(2H)-dione, with the CAS number 70478-63-6, is a chemical compound characterized by its isoindole structure, which features a fused benzene and pyrrole ring system. The presence of a bromine atom at the 4-position contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. This compound typically exhibits a solid state at room temperature and is known for its stability under standard conditions. It is often utilized in research for its potential biological activities, including antimicrobial and anticancer properties. The dione functional groups in its structure suggest the ability to participate in various chemical reactions, such as nucleophilic additions and cycloadditions. Its solubility may vary depending on the solvent, but it is generally more soluble in organic solvents than in water. As with many brominated compounds, safety precautions should be taken due to potential toxicity and environmental impact. Overall, 4-bromo-1H-isoindole-1,3(2H)-dione is a compound of interest in both synthetic and medicinal chemistry.

CAS 70478-63-6

4-bromo-1H-isoindole-1,3(2H)-dione

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