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Structure of 396074-50-3
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This chiral oxathiazolidine derivative features a tert-butyl ester-protected carboxylic acid and a methyl-substituted sulfur-nitrogen heterocycle. The scaffold delivers stereochemical control in synthetic sequences involving cysteine analogs or thioether incorporation. Bench-stable under standard conditions, it integrates seamlessly into peptide mimetics and bioactive molecule synthesis.
(S)-5-Methyl-2,2-dioxo-[1,2,3]oxathiazolidine-3-carboxylic acid tert-butyl ester serves as a stable, bench-ready chiral building block for sulfur-containing heterocycles. Its sulfonamide-like functionality enables reliable participation in nucleophilic substitution and cyclization reactions, while the tert-butyl ester group provides excellent stability and straightforward deprotection under mild acidic conditions. This compound facilitates the synthesis of complex thiazolidine-based scaffolds relevant to medicinal chemistry and catalytic system development.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: