tert-Butyl (S)-4-(((tert-butyldimethylsilyl)oxy)methyl)-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide

95%

Reagent Code: #152791
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CAS Number 1338090-89-3

science Other reagents with same CAS 1338090-89-3

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inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral auxiliary and intermediate in the synthesis of biologically active molecules, particularly in asymmetric synthesis where stereocontrol is critical. Its structure allows for selective transformations, especially in the preparation of β-amino alcohols and other nitrogen-containing compounds. The silyl protecting group enhances stability and solubility in organic solvents, facilitating multi-step synthetic routes. Commonly employed in medicinal chemistry for the development of protease inhibitors and other pharmaceuticals requiring high enantiomeric purity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,350.00
inventory 250mg
10-20 days ฿36,280.00
inventory 1g
10-20 days ฿97,890.00

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tert-Butyl (S)-4-(((tert-butyldimethylsilyl)oxy)methyl)-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide
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Used as a chiral auxiliary and intermediate in the synthesis of biologically active molecules, particularly in asymmetric synthesis where stereocontrol is critical. Its structure allows for selective transformations, especially in the preparation of β-amino alcohols and other nitrogen-containing compounds. The silyl protecting group enhances stability and solubility in organic solvents, facilitating multi-step synthetic routes. Commonly employed in medicinal chemistry for the development of protease inhibit
Used as a chiral auxiliary and intermediate in the synthesis of biologically active molecules, particularly in asymmetric synthesis where stereocontrol is critical. Its structure allows for selective transformations, especially in the preparation of β-amino alcohols and other nitrogen-containing compounds. The silyl protecting group enhances stability and solubility in organic solvents, facilitating multi-step synthetic routes. Commonly employed in medicinal chemistry for the development of protease inhibitors and other pharmaceuticals requiring high enantiomeric purity.
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