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Structure of 942919-26-8
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine features a boronate ester group flanked by a tetramethyl-substituted dioxaborolane ring, enabling stable coupling in Suzuki-Miyaura reactions. The electron-deficient pyrrolo[2,3-b]pyridine core integrates readily into heterocyclic scaffolds under standard conditions. This bench-stable reagent streamlines access to complex nitrogen-rich architectures.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine serves as a versatile boronate building block in palladium-catalyzed cross-coupling reactions. Its stability under ambient conditions and compatibility with diverse functional groups enable efficient construction of biaryl architectures. The tetramethyl-substituted dioxaborolane moiety facilitates reliable coupling with aryl halides and pseudohalides, making it well-suited for synthesizing complex heterocyclic scaffolds in 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: