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Structure of 1315281-29-8
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This boronate-functionalized imidazole integrates readily into Suzuki-Miyaura coupling reactions under standard conditions, delivering stable heterocyclic scaffolds with enhanced reaction efficiency. The tetramethyl-substituted dioxaborolane moiety ensures excellent shelf stability and moisture tolerance, while the 2-chloro-1-methyl substitution pattern enables selective transformations in complex molecular architectures.
2-Chloro-1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazole serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylboronate group enables efficient palladium-catalyzed coupling with aryl and vinyl halides, while the 2-chloroimidazole core provides a stable, functionalized scaffold for medicinal chemistry applications. Bench-stable and readily purified by flash chromatography, it facilitates the construction of complex imidazole-based heterocycles in multi-step synthesis.
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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: