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Structure of 1233542-00-1
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7-Bromo-1-methyl-1H-benzo[d]imidazole features a brominated benzene ring fused to a methylated imidazole core, delivering enhanced electron-withdrawing character and improved solubility in organic solvents. This scaffold enables efficient coupling reactions in transition-metal-catalyzed transformations, serving as a stable building block for bioactive heterocycles and functional materials.
7-Bromo-1-methyl-1H-benzo[d]imidazole serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. Its bromine substituent enables palladium-catalyzed cross-coupling reactions, while the methylated imidazole core provides enhanced stability and solubility. The compound functions effectively in Suzuki-Miyaura and Buchwald-Hartwig couplings, facilitating rapid access to complex biaryl and amine-containing scaffolds. Bench-stable and readily purified by recrystallization, it supports scalable synthesis of functionalized nitrogen heterocycles relevant to pharmaceutical development.
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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: