4-Chloroisoindoline is a chemical compound characterized by its isoindoline structure, which consists of a bicyclic system featuring a five-membered ring fused to a six-membered ring. The presence of a chlorine atom at the 4-position of the isoindoline ring significantly influences its chemical properties and reactivity. This compound typically exhibits a pale yellow to brownish color and is known for its potential applications in organic synthesis and medicinal chemistry. It may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the electron-withdrawing nature of the chlorine substituent. Additionally, 4-chloroisoindoline may exhibit biological activity, making it of interest in pharmaceutical research. Its solubility and stability can vary depending on the solvent and environmental conditions. As with many organic compounds, safety precautions should be observed when handling this substance, as it may pose health risks if ingested or inhaled. Overall, 4-chloroisoindoline is a versatile compound with significant implications in both research and industrial applications.

4-CHLOROISOINDOLINE

123594-04-7: 4-Chloroisoindoline is a chemical compound characterized by its isoindoline structure, which consists of a bicyclic system featuring a five-membered ring fused to a six-membered ring. The presence of a chlorine atom at the 4-position of the isoindoline ring significantly influences its chemical properties and reactivity. This compound typically exhibits a pale yellow to brownish color and is known for its potential applications in organic synthesis and medicinal chemistry. It may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the electron-withdrawing nature of the chlorine substituent. Additionally, 4-chloroisoindoline may exhibit biological activity, making it of interest in pharmaceutical research. Its solubility and stability can vary depending on the solvent and environmental conditions. As with many organic compounds, safety precautions should be observed when handling this substance, as it may pose health risks if ingested or inhaled. Overall, 4-chloroisoindoline is a versatile compound with significant implications in both research and industrial applications.

CAS 123594-04-7

4-CHLOROISOINDOLINE

1H-Isoindole, 4-chloro-2,3-dihydro-

Ref: IN-DA000KU5

4-Chloroisoindoline

Ref: 10-F220119