5-Hydroxyisoindolin-1-one is an organic compound characterized by its isoindoline structure, which features a fused benzene and pyrrole ring system. This compound contains a hydroxyl group (-OH) at the 5-position of the isoindoline ring, contributing to its chemical reactivity and potential biological activity. It is typically a white to off-white solid and is soluble in polar solvents, which can facilitate its use in various chemical reactions and applications. The presence of the hydroxyl group can enhance its ability to participate in hydrogen bonding, influencing its solubility and interaction with other molecules. 5-Hydroxyisoindolin-1-one has garnered interest in medicinal chemistry due to its potential pharmacological properties, including anti-inflammatory and neuroprotective effects. Its unique structure allows for further derivatization, making it a valuable scaffold in drug design. As with many organic compounds, proper handling and storage are essential to maintain its stability and efficacy in research and application settings.

5-hydroxyisoindolin-1-one

252061-66-8: 5-Hydroxyisoindolin-1-one is an organic compound characterized by its isoindoline structure, which features a fused benzene and pyrrole ring system. This compound contains a hydroxyl group (-OH) at the 5-position of the isoindoline ring, contributing to its chemical reactivity and potential biological activity. It is typically a white to off-white solid and is soluble in polar solvents, which can facilitate its use in various chemical reactions and applications. The presence of the hydroxyl group can enhance its ability to participate in hydrogen bonding, influencing its solubility and interaction with other molecules. 5-Hydroxyisoindolin-1-one has garnered interest in medicinal chemistry due to its potential pharmacological properties, including anti-inflammatory and neuroprotective effects. Its unique structure allows for further derivatization, making it a valuable scaffold in drug design. As with many organic compounds, proper handling and storage are essential to maintain its stability and efficacy in research and application settings.

CAS 252061-66-8

5-hydroxyisoindolin-1-one

1H-Isoindol-1-one, 2,3-dihydro-5-hydroxy-

Ref: IN-DA002QXJ

5-Hydroxyisoindolin-1-one

Ref: 54-OR305282

5-Hydroxyisoindolin-1-one

Ref: 10-F220172