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Structure of 530081-14-2
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1-(4-Bromophenyl)imidazolidin-2-one features a brominated aromatic ring fused to a rigid imidazolidin-2-one core, delivering enhanced stability and targeted reactivity. This bench-stable scaffold integrates readily into medicinal chemistry libraries, enabling efficient access to bioactive compounds through direct functionalization at the bromo site.
1-(4-Bromophenyl)imidazolidin-2-one serves as a versatile building block in medicinal chemistry, enabling the synthesis of imidazolidinone-based scaffolds via standard functional group transformations. The bromo substituent facilitates palladium-catalyzed cross-coupling reactions, while the imidazolidinone core provides structural rigidity and hydrogen-bonding capability. Bench-stable and readily purified by recrystallization, it functions effectively in multi-step syntheses requiring orthogonal reactivity and compatibility with diverse reaction conditions.
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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: