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Structure of 23328-88-3
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2-Bromo-4-methyl-1H-imidazole is a bench-stable heterocyclic building block featuring a bromine substituent at the 2-position and a methyl group at the 4-position, enabling direct functionalization in cross-coupling reactions. The imidazole core provides strong coordination potential and enhanced solubility in polar solvents, facilitating use in synthetic medicinal chemistry and catalytic system development.
2-Bromo-4-methyl-1H-imidazole serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C2 position via palladium-catalyzed cross-coupling reactions. Its stability under standard synthetic conditions and tolerance to common functional groups facilitate efficient access to substituted imidazoles. The methyl group enhances regioselectivity in downstream transformations, making it particularly valuable for constructing bioactive heterocyclic scaffolds in drug discovery workflows.
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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: