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Structure of 1525619-20-8
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2-Bromo-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole is a heterocyclic scaffold featuring a brominated imidazole core with enhanced stability and tunable reactivity. This bench-stable compound integrates readily into transition-metal-catalyzed coupling reactions, enabling efficient access to functionalized pyrroloimidazoles for medicinal chemistry applications.
2-Bromo-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole serves as a versatile building block for the synthesis of functionalized purine analogs and heterocyclic scaffolds. The bromine substituent enables palladium-catalyzed cross-coupling reactions, facilitating C–C bond formation under mild conditions. Its saturated imidazole core provides enhanced stability and solubility compared to aromatic counterparts, while maintaining compatibility with standard protecting group strategies. This compound functions effectively in late-stage diversification workflows common in medicinal chemistry.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: