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Structure of 1254697-46-5
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-3H-imidazo[4,5-b]pyridine features a boronate ester handle fused to an electron-rich imidazopyridine core, enabling efficient cross-coupling reactions under mild conditions. This bench-stable reagent integrates seamlessly into Suzuki-Miyaura protocols for constructing complex heterocyclic scaffolds in medicinal chemistry and materials science.
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-3H-imidazo[4,5-b]pyridine serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. Its stable tetramethylboronate group enables efficient Suzuki-Miyaura coupling with aryl and heteroaryl halides, facilitating rapid assembly of biaryl architectures. The imidazopyridine core provides a rigid, electron-deficient scaffold useful in medicinal chemistry and materials science. Bench-stable and readily purified by flash chromatography, it functions reliably in standard synthetic workflows.
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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: