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Structure of 13380-67-1
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1-(4-Bromophenyl)-1H-pyrrole-2,5-dione features a brominated aromatic ring fused to a maleimide core, enabling direct incorporation into conjugation workflows. This electron-deficient diene serves as a robust Michael acceptor in bioconjugation and polymer synthesis, offering high reactivity under mild conditions with nucleophilic side chains. The bench-stable crystalline solid facilitates handling and storage without degradation.
1-(4-Bromophenyl)-1H-pyrrole-2,5-dione serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of functionalized heterocycles and conjugated systems. Its brominated aryl moiety facilitates palladium-catalyzed cross-coupling reactions, while the maleimide core offers robust functionality for Diels–Alder cycloadditions and nucleophilic additions. The compound exhibits excellent bench stability and simplifies purification, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: