N-p-Toluenesulfonylimino-3,3’-Dipropionic Acid

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Reagent Code: #220230
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CAS Number 5446-58-2

science Other reagents with same CAS 5446-58-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.34 g/mol
Formula C₁₃H₁₇NO₆S
badge Registry Numbers
MDL Number MFCD00045941
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key reagent in organic synthesis, particularly in the preparation of aziridines through the aziridination of alkenes. It serves as a source of the nitrene group in metal-catalyzed reactions, enabling the formation of three-membered nitrogen-containing rings which are valuable intermediates in pharmaceutical and agrochemical synthesis. Its stability and reactivity profile make it suitable for selective transformations in complex molecule assembly. Commonly employed in research settings for C–H amination and heterocycle formation.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿14,690.00
inventory 5g
10-20 days ฿73,430.00

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N-p-Toluenesulfonylimino-3,3’-Dipropionic Acid
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Used as a key reagent in organic synthesis, particularly in the preparation of aziridines through the aziridination of alkenes. It serves as a source of the nitrene group in metal-catalyzed reactions, enabling the formation of three-membered nitrogen-containing rings which are valuable intermediates in pharmaceutical and agrochemical synthesis. Its stability and reactivity profile make it suitable for selective transformations in complex molecule assembly. Commonly employed in research settings for C–H a

Used as a key reagent in organic synthesis, particularly in the preparation of aziridines through the aziridination of alkenes. It serves as a source of the nitrene group in metal-catalyzed reactions, enabling the formation of three-membered nitrogen-containing rings which are valuable intermediates in pharmaceutical and agrochemical synthesis. Its stability and reactivity profile make it suitable for selective transformations in complex molecule assembly. Commonly employed in research settings for C–H amination and heterocycle formation.

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