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Structure of 1964-77-8
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5-Bromo-2-methyl-1H-benzo[d]imidazole features a brominated benzene ring fused to an imidazole core, delivering enhanced electron-withdrawing character and site-specific reactivity. The methyl group at the 2-position provides steric stabilization, while the bromine enables facile cross-coupling transformations. This bench-stable heterocycle serves as a key building block in medicinal chemistry and materials synthesis.
5-Bromo-2-methyl-1H-benzo[d]imidazole serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent. The methyl group at the 2-position enhances electronic stability and facilitates regioselective functionalization. This compound exhibits good bench stability and is compatible with standard synthetic workflows, making it valuable for constructing biologically active heterocyclic scaffolds and pharmaceutical intermediates.
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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: