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Structure of 212127-83-8
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tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,5-dihydro-1H-pyrrole-1-carboxylate features a stable boronate ester integrated into a dihydropyrrole scaffold, enabling direct coupling in Suzuki-Miyaura reactions. This bench-stable reagent streamlines access to functionalized pyrrole derivatives with minimal handling complexity.
tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,5-dihydro-1H-pyrrole-1-carboxylate serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. The dioxaborolane moiety enables efficient coupling with aryl and vinyl halides under mild conditions, while the protected pyrrolidine scaffold offers orthogonal functional group compatibility. Its high stability, ease of handling, and predictable reactivity make it ideal for constructing complex heterocyclic frameworks in medicinal chemistry and materials synthesis.
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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: