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Structure of 1095708-32-9
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This boronate ester features a pyridine core functionalized with a tert-butyl carbamate and a tetramethylboronate group, enabling efficient cross-coupling under mild conditions. The protecting group remains stable during reaction setup and can be removed post-functionalization, streamlining access to diverse nitrogen-containing scaffolds in medicinal chemistry and materials science.
tert-Butyl (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)carbamate serves as a stable, bench-friendly boron building block for Suzuki-Miyaura cross-coupling reactions. The pyridine scaffold enables versatile functionalization in medicinal chemistry and materials science, while the Boc-protected amine ensures compatibility with diverse reaction conditions. Its high functional group tolerance and ease of purification streamline synthetic 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-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: