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Structure of 214360-77-7
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This boronate-functionalized pyrrole integrates readily into Suzuki-Miyaura coupling reactions under standard conditions, offering high stability and compatibility with diverse reaction partners. The tetramethylcyclopentadienone-derived boronate moiety enables efficient cross-coupling while maintaining bench-stable handling characteristics.
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. The tetramethyl-substituted dioxaborolane moiety enhances air and moisture stability while enabling efficient palladium-catalyzed coupling with aryl and heteroaryl halides. Its compatibility with diverse functional groups makes it a practical tool for constructing biologically relevant pyrrole-containing 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: