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Structure of 88511-13-1
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This sulfone-containing heterocycle features a nitrogen-substituted thietane ring, delivering enhanced stability and polarity. The 3-amino group enables direct functionalization in synthetic sequences, while the 1,1-dioxide moiety imparts strong electron-withdrawing character. Ideal for incorporating into bioactive scaffolds and polar reaction intermediates under standard conditions.
3-Aminothietane 1,1-dioxide serves as a versatile sulfonamide-containing building block in medicinal chemistry, enabling efficient access to bioactive heterocycles. Its stable, bench-ready nature and compatibility with standard coupling reactions facilitate straightforward incorporation into complex molecular architectures. The molecule functions effectively in the synthesis of sulfonamide-based pharmacophores and provides a reliable scaffold for exploring structure-activity relationships in drug discovery programs.
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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: