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Structure of 935455-28-0
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This chiral sulfonamide scaffold delivers a rigid, bench-stable platform for asymmetric synthesis. The (S)-configured tetrahydrothiophene core bears a protonated amine and two sulfonyl oxygens, enabling strong hydrogen bonding and enhanced solubility in aqueous-organic mixtures. Ideal for medicinal chemistry campaigns requiring stereocontrolled heterocyclic motifs with improved metabolic stability.
(S)-3-Aminotetrahydrothiophene 1,1-dioxide hydrochloride serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of sulfonamide-containing heterocycles. Its stable, bench-ready form facilitates straightforward handling and purification, while the amino group supports diverse functionalization including coupling reactions and derivatization. The sulfone moiety imparts enhanced metabolic stability and polarity, making it well-suited for constructing bioactive scaffolds 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: