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Structure of 255064-10-9
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5-Bromo-7-methyl-1H-benzo[d]imidazole features a bromine atom at the 5-position and a methyl group at the 7-position, conferring enhanced electrophilic reactivity and improved solubility in organic media. This scaffold integrates readily into heterocyclic architectures, enabling efficient coupling in transition-metal-catalyzed transformations. Its bench-stable nature facilitates handling under standard conditions.
5-Bromo-7-methyl-1H-benzo[d]imidazole serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent. The methyl group enhances solubility and provides a handle for further functionalization. Its stability under standard reaction conditions and compatibility with common coupling protocols make it a practical choice for constructing biologically relevant scaffolds 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: