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Structure of 1008361-65-6
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5-Bromo-6-methoxy-1H-benzo[d]imidazole integrates a bromine electrophile and methoxy donor within a rigid heterocyclic scaffold, enabling direct functionalization in cross-coupling reactions. This bench-stable, moisture-tolerant imidazole derivative facilitates efficient access to substituted bioactive scaffolds under standard conditions.
5-Bromo-6-methoxy-1H-benzo[d]imidazole serves as a versatile building block for the synthesis of bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo group and orthogonal methoxy functionality. The molecule exhibits excellent bench stability, facilitates straightforward purification, and functions effectively in standard Suzuki-Miyaura and Buchwald-Hartwig coupling protocols, making it well-suited for 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: