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Structure of 1248548-54-0
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7-Bromo-2-chloro-1H-benzo[d]imidazole features a fused heterocyclic core with complementary halogen substituents enabling precise functionalization. The bromine and chlorine atoms facilitate palladium-catalyzed cross-coupling reactions, while the electron-deficient imidazole ring enhances reactivity in C–H activation and transition-metal-mediated transformations. This scaffold serves as a robust building block for bioactive molecules and advanced materials.
7-Bromo-2-chloro-1H-benzo[d]imidazole serves as a versatile heterocyclic building block in medicinal chemistry and materials science. Its dual halogenation pattern enables palladium-catalyzed cross-coupling reactions, including Suzuki-Miyaura and Buchwald-Hartwig aminations, with high functional group tolerance. The molecule exhibits excellent bench stability and facilitates efficient purification, making it well-suited for modular synthesis of biologically active scaffolds and advanced organic semiconductors.
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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-H320-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: