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396074-50-3

1,2,3-Oxathiazolidine-3-carboxylic acid, 5-methyl-, 1,1-dimethylethylester, 2,2-dioxide, (5S)-

Catalog#: AR00I8HB  |   CAS#: 396074-50-3  |   MDL#: MFCD09833247  |   MF: C8H15NO5S  |   MW: 237.2734

Packsize Purity Price Availability Quantity
100mg 97% $5.00 Global Stock Buy Now Add To Cart
250mg 97% $6.00 Global Stock Buy Now Add To Cart
1g 97% $18.00 Global Stock Buy Now Add To Cart
5g 97% $70.00 Global Stock Buy Now Add To Cart
10g 97% $118.00 Global Stock Buy Now Add To Cart
25g 97% $243.00 Global Stock Buy Now Add To Cart
50g 97% $450.00 Global Stock Buy Now Add To Cart
100g 97% $693.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00I8HB
Chemical Name 1,2,3-Oxathiazolidine-3-carboxylic acid, 5-methyl-, 1,1-dimethylethylester, 2,2-dioxide, (5S)-
CAS Number 396074-50-3
Molecular Formula C8H15NO5S
Molecular Weight 237.2734
MDL Number MFCD09833247
SMILES C[C@H]1CN(S(=O)(=O)O1)C(=O)OC(C)(C)C

(S)-tert-Butyl 5-methyl-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide is a valuable compound widely utilized in chemical synthesis processes. This compound serves as a chiral building block in organic reactions, particularly in the formation of asymmetric compounds. Its unique structure containing an oxathiazolidine ring and a tert-butyl group imparts specificity and stereochemical control in various synthetic pathways.In chemical synthesis, (S)-tert-Butyl 5-methyl-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide is commonly employed in the production of pharmaceutical intermediates, agrochemicals, and specialty chemicals. Its chirality allows for the creation of enantiomerically pure products, which are crucial in the pharmaceutical industry to ensure desired biological activity and minimize side effects.Moreover, this compound can function as a protecting group for amines during chemical transformations, shielding them from unwanted reactions and enabling selective modifications at specific positions within a molecule. By incorporating (S)-tert-Butyl 5-methyl-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide into synthetic routes, chemists can efficiently access complex molecules with high stereoselectivity, paving the way for the development of novel compounds with diverse applications.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P280-P301+P312-P302+P352-P305+P351+P338
Class -
Packing Group -

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