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Structure of 39513-26-3
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5-Bromo-1,3-dihydrobenzoimidazol-2-one features a brominated benzene ring fused to a labile imidazolone core, enabling direct functionalization at the C5 position. This electron-deficient heterocycle serves as a stable scaffold for late-stage derivatization in medicinal chemistry and materials synthesis.
5-Bromo-1,3-dihydrobenzoimidazol-2-one serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted benzimidazoles via palladium-catalyzed cross-coupling reactions. The bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, while the lactam functionality offers orthogonal handle for further functionalization. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step sequences requiring good functional group tolerance and predictable regiochemistry.
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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: