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Structure of 945256-29-1
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This boronate-functionalized pyrrolopyridine integrates readily into Suzuki-Miyaura coupling reactions under standard conditions. The tetramethylborolane moiety ensures high stability and compatibility with diverse reaction environments, enabling efficient C–C bond formation in synthetic sequences.
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. Its pyrrolo[2,3-b]pyridine core provides a rigid, electron-deficient heterocyclic scaffold commonly found in bioactive molecules. The pinacol boronate group enables excellent bench stability, facile purification, and compatibility with diverse reaction conditions, facilitating efficient construction of complex scaffolds in medicinal chemistry and materials science.
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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: