(R)-3-Boc-4-methyl-1,2,3-oxathiazolidine 2,2-Dioxide

98%

Reagent Code: #230732
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CAS Number 454248-53-4

science Other reagents with same CAS 454248-53-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.27 g/mol
Formula C₈H₁₅NO₅S
badge Registry Numbers
MDL Number MFCD09864994
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure sulfonamides and sulfoxides. Its rigid cyclic structure and defined stereochemistry allow for high stereoselectivity in nucleophilic addition and substitution reactions. Commonly employed in pharmaceutical intermediates synthesis where control of stereochemistry is critical, such as in the development of protease inhibitors or other bioactive molecules. The Boc group provides stability and ease of deprotection under mild acidic conditions, making it suitable for multi-step synthetic sequences.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿700.00
inventory 5g
10-20 days ฿2,760.00
inventory 10g
10-20 days ฿4,820.00
inventory 25g
10-20 days ฿11,690.00
inventory 100g
10-20 days ฿34,350.00
(R)-3-Boc-4-methyl-1,2,3-oxathiazolidine 2,2-Dioxide
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Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure sulfonamides and sulfoxides. Its rigid cyclic structure and defined stereochemistry allow for high stereoselectivity in nucleophilic addition and substitution reactions. Commonly employed in pharmaceutical intermediates synthesis where control of stereochemistry is critical, such as in the development of protease inhibitors or other bioactive molecules. The Boc group provides stability and ease of

Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure sulfonamides and sulfoxides. Its rigid cyclic structure and defined stereochemistry allow for high stereoselectivity in nucleophilic addition and substitution reactions. Commonly employed in pharmaceutical intermediates synthesis where control of stereochemistry is critical, such as in the development of protease inhibitors or other bioactive molecules. The Boc group provides stability and ease of deprotection under mild acidic conditions, making it suitable for multi-step synthetic sequences.

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