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Structure of 1003-91-4
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2,4,5-Tribromo-1-methyl-1H-imidazole features a highly brominated imidazole core with methyl substitution, delivering enhanced reactivity in cross-coupling and electrophilic functionalization. The dense halogenation pattern enables efficient C–X bond formation under mild conditions, while the methyl group improves solubility and stability. This compound serves as a robust scaffold for synthesizing complex heterocyclic architectures in medicinal chemistry and materials science.
2,4,5-Tribromo-1-methyl-1H-imidazole serves as a versatile brominated building block for the synthesis of functionalized imidazoles and heterocyclic scaffolds. Its high reactivity in palladium-catalyzed cross-coupling reactions enables efficient C–C and C–heteroatom bond formation under mild conditions. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic strategies 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: