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Structure of 454248-53-4
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(R)-tert-Butyl 4-methyl-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide features a chiral oxathiazolidine scaffold with a bench-stable sulfone moiety and a sterically protected tert-butyl ester. This configuration delivers high diastereoselectivity in asymmetric synthesis, enabling efficient incorporation of sulfur-containing motifs into complex molecular architectures under mild conditions.
(R)-tert-Butyl 4-methyl-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide serves as a stable, bench-ready chiral synthon for sulfur-containing heterocycles. Its sulfonamide-like reactivity enables efficient nucleophilic displacement and transition-metal-catalyzed transformations. The oxathiazolidine core provides excellent functional group tolerance and facilitates stereoselective C–X bond formation, making it valuable in the synthesis of complex intermediates for medicinal chemistry and catalytic process 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-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: