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Structure of 935278-73-2
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tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate features a boronate ester group integrated into a pyrrole scaffold, enabling efficient cross-coupling reactions. The tetramethyl-substituted dioxaborolane moiety enhances stability and reactivity under standard conditions. This bench-stable reagent facilitates the construction of complex heterocyclic architectures in synthetic and medicinal chemistry workflows.
tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate serves as a stable, bench-friendly boron building block for palladium-catalyzed cross-coupling reactions. The tetramethylborolane moiety enables efficient Suzuki-Miyaura coupling under mild conditions, while the tert-butyl ester provides orthogonal protection and facile deprotection. This reagent facilitates rapid access to functionalized pyrrole scaffolds prevalent 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: