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Structure of 1351379-23-1
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Methyl 1-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-2-carboxylate features a boronate ester group integrated into a pyrrole scaffold, enabling efficient cross-coupling reactions. The tetramethyl-1,3,2-dioxaborolane moiety imparts enhanced stability and compatibility under standard reaction conditions. This bench-stable reagent streamlines the construction of complex heterocyclic architectures in synthetic organic chemistry and medicinal discovery.
Methyl 1-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-2-carboxylate serves as a versatile boron building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylboronate group enables efficient coupling with aryl and heteroaryl halides under mild conditions, while the pyrrole core provides a platform for constructing biologically relevant heterocyclic scaffolds. Bench-stable and compatible with diverse functional groups, it facilitates rapid access to complex molecular architectures in medicinal chemistry and materials science 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: