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Structure of 850429-59-3
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4-Bromo-1,2-dimethyl-1H-imidazole features a brominated imidazole core with methyl groups at the 1- and 2-positions, delivering enhanced stability and tailored reactivity. This electron-deficient heterocycle integrates readily into cross-coupling reactions and serves as a key building block in medicinal chemistry and agrochemical synthesis.
4-Bromo-1,2-dimethyl-1H-imidazole serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo functionality. The methyl groups at C1 and C2 enhance solubility and reduce undesired side reactivity, while the imidazole core provides a robust scaffold for bioactive molecule construction. Its bench-stable nature and ease of purification make it well-suited for scalable synthesis and parallel library development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: