4-Chloro-1H-isoindole-1,3(2H)-dione, also known as phthalimide derivative, is an organic compound characterized by its isoindole structure, which features a five-membered ring fused to a six-membered aromatic ring. This compound contains a chlorine substituent at the 4-position and two carbonyl groups, contributing to its reactivity and potential applications in organic synthesis. It is typically a white to off-white solid, exhibiting moderate solubility in organic solvents such as dichloromethane and dimethyl sulfoxide, but limited solubility in water. The presence of the chloro group enhances its electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions and cycloadditions. Additionally, the compound may exhibit biological activity, which has led to interest in its potential as a pharmaceutical intermediate. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 4-chloro-1H-isoindole-1,3(2H)-dione is a versatile compound with significant implications in both synthetic chemistry and medicinal research.

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

51108-30-6: 4-Chloro-1H-isoindole-1,3(2H)-dione, also known as phthalimide derivative, is an organic compound characterized by its isoindole structure, which features a five-membered ring fused to a six-membered aromatic ring. This compound contains a chlorine substituent at the 4-position and two carbonyl groups, contributing to its reactivity and potential applications in organic synthesis. It is typically a white to off-white solid, exhibiting moderate solubility in organic solvents such as dichloromethane and dimethyl sulfoxide, but limited solubility in water. The presence of the chloro group enhances its electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions and cycloadditions. Additionally, the compound may exhibit biological activity, which has led to interest in its potential as a pharmaceutical intermediate. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 4-chloro-1H-isoindole-1,3(2H)-dione is a versatile compound with significant implications in both synthetic chemistry and medicinal research.

CAS 51108-30-6

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

4-chloroisoindole-1,3-dione

Ref: IN-DA00DL3Q

4-Chloroisoindoline-1,3-dione

Ref: 54-OR1059374

1H-ISOINDOLE-1,3(2H)-DIONE, 4-CHLORO-

Ref: 10-F468996