N-Ethyl-3-phenyl-1,2-oxaziridine-2-carboxamide

95%

Reagent Code: #218769
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CAS Number 2089059-42-5

science Other reagents with same CAS 2089059-42-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.2 g/mol
Formula C₁₀H₁₂N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, dry, closed

description Product Description

Used primarily as a chiral oxidizing agent in organic synthesis, this compound enables selective epoxidation of alkenes and oxidation of sulfides to sulfoxides with high enantioselectivity. Its strained oxaziridine ring facilitates oxygen transfer under mild conditions, making it valuable in the preparation of pharmaceutical intermediates and fine chemicals where stereochemical control is critical. It is also employed in the synthesis of bioactive molecules, including natural products and drug candidates, due to its ability to introduce oxygen atoms with predictable stereochemistry. The ethyl and phenyl substituents enhance stability and influence reactivity and selectivity in asymmetric transformations.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿65,210.00
N-Ethyl-3-phenyl-1,2-oxaziridine-2-carboxamide
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Used primarily as a chiral oxidizing agent in organic synthesis, this compound enables selective epoxidation of alkenes and oxidation of sulfides to sulfoxides with high enantioselectivity. Its strained oxaziridine ring facilitates oxygen transfer under mild conditions, making it valuable in the preparation of pharmaceutical intermediates and fine chemicals where stereochemical control is critical. It is also employed in the synthesis of bioactive molecules, including natural products and drug candidates

Used primarily as a chiral oxidizing agent in organic synthesis, this compound enables selective epoxidation of alkenes and oxidation of sulfides to sulfoxides with high enantioselectivity. Its strained oxaziridine ring facilitates oxygen transfer under mild conditions, making it valuable in the preparation of pharmaceutical intermediates and fine chemicals where stereochemical control is critical. It is also employed in the synthesis of bioactive molecules, including natural products and drug candidates, due to its ability to introduce oxygen atoms with predictable stereochemistry. The ethyl and phenyl substituents enhance stability and influence reactivity and selectivity in asymmetric transformations.

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