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Structure of 1609964-38-6
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tert-Butyl 1-iminothiomorpholine-4-carboxylate 1-oxide features a sulfimide-functionalized heterocycle with enhanced stability and tunable reactivity. This bench-stable oxidized scaffold integrates readily into synthetic sequences requiring nitrogen-centered radical precursors or electrophilic building blocks. The tert-butyl ester group enables straightforward deprotection under mild acidic conditions, facilitating downstream functionalization in complex molecule assembly.
tert-Butyl 1-iminothiomorpholine-4-carboxylate 1-oxide serves as a stable, bench-ready building block for the synthesis of thiomorpholine-based heterocycles. Its oxidized imino functionality enables selective transformations in late-stage functionalization, while the tert-butyl ester facilitates straightforward deprotection under mild acidic conditions. The molecule exhibits excellent functional group tolerance and compatibility with standard coupling and reduction protocols, making it valuable for medicinal chemistry campaigns targeting sulfur-containing scaffolds.
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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: