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Structure of 1613373-40-2
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This imidazolidinedione derivative features a brominated aryl group flanked by two methyl substituents, enhancing electronic and steric profile. The 5,5-dimethyl substitution confers stability and solubility advantages. It serves as a robust building block in medicinal chemistry for constructing complex heterocyclic scaffolds under standard conditions.
1-(4-Bromo-3,5-dimethylphenyl)-5,5-dimethylimidazolidine-2,4-dione serves as a versatile building block for the synthesis of substituted benzimidazoles and related heterocyclic scaffolds. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the dimethyl-substituted imidazolidinedione core offers enhanced bench stability and facilitates purification. This compound functions effectively in standard medicinal chemistry workflows, providing reliable access to complex molecular architectures through well-established transformation pathways.
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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: