N-(4-Acetylphenyl)maleimide, with the CAS number 1082-85-5, is an organic compound characterized by its maleimide structure, which is a five-membered cyclic imide. This compound features an acetyl group attached to the para position of a phenyl ring, contributing to its reactivity and solubility properties. It is typically a white to light yellow crystalline solid, exhibiting moderate solubility in organic solvents such as acetone and dichloromethane, while being less soluble in water. N-(4-Acetylphenyl)maleimide is known for its ability to undergo Michael addition reactions, making it useful in various applications, including polymer chemistry and organic synthesis. Its reactivity allows it to form adducts with nucleophiles, which is valuable in the development of functional materials and in the modification of polymers. Additionally, this compound may exhibit biological activity, although specific biological properties would depend on the context of its use. Proper handling and storage are essential due to its potential reactivity and the need for safety precautions in laboratory settings.

N-(4-Acetylphenyl)maleimide

1082-85-5: Maleimide, N-(p-acetylphenyl)-, N-(p-Acetylphenyl)maleimide, N-(4-Acetylphenyl)maleimide, 1H-Pyrrole-2,5-dione, 1-(4-acetylphenyl)-, 1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione

1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione

N-(4-ACETYLPHENYL)MALEIMIDE

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CAS 1082-85-5: N-(4-Acetylphenyl)maleimide

1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione

Ref: 54-OR4948

N-(4-ACETYLPHENYL)MALEIMIDE

Ref: IN-DA003SBK

N-(4-Acetylphenyl)maleimide

Ref: 10-F011070

N-(4-Acetylphenyl)maleimide

Ref: 3D-FA168814