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Structure of 1451153-83-5
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This tetrahydropyridylboronic acid features a tert-butoxycarbonyl-protected nitrogen, enabling stable handling and selective deprotection during synthesis. The boronic acid moiety integrates readily into Suzuki-Miyaura couplings, while the electron-rich tetrahydropyridine scaffold enhances reactivity in transition-metal-catalyzed transformations.
{1-[(tert-Butoxy)carbonyl]-1,2,5,6-tetrahydropyridin-3-yl}boronic acid serves as a stable, bench-friendly building block for the synthesis of nitrogen-containing heterocycles and bioactive scaffolds. Its tetrahydropyridine core enables diverse Suzuki-Miyaura coupling reactions with excellent functional group tolerance. The Boc-protected amine facilitates orthogonal manipulation in multi-step sequences, while the boronic acid moiety supports efficient purification and compatibility with standard aqueous workups.
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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: