2-[N,N-Bis(trifluoromethylsulfonyl)amino]pyridine

95%

Reagent Code: #217106
label
Alias N-(2-pyridinyl)bis(trifluoromethanesulfonylimide)[trifluoromethylsulfonyl]; 2-[N,n-bis(trifluoromethanesulfonyl)amino]pyridine; N,N-bis(trifluoromethanesulfonyl)-2-pyridinylamine
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CAS Number 145100-50-1

science Other reagents with same CAS 145100-50-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 358.23 g/mol
Formula C₇H₄F₆N₂O₄S₂
badge Registry Numbers
MDL Number MFCD00191834
thermostat Physical Properties
Melting Point 40-42 °C (Lit.)
Boiling Point 80-90 °C/0.25 mmHg (lit.)
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a highly effective reagent in organic synthesis, particularly as a precursor for generating electrophilic aminating agents. It plays a key role in the preparation of nitrogen-containing compounds through electrophilic amination of carbon nucleophiles. Commonly employed in the synthesis of heterocycles and functionalized amines, which are important in pharmaceutical and agrochemical industries. Its strong electron-withdrawing sulfonyl groups enhance reactivity and stability of intermediates, making it valuable in transition metal-catalyzed reactions and modern C–H functionalization processes.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,170.00
inventory 25g
10-20 days ฿3,162.00

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2-[N,N-Bis(trifluoromethylsulfonyl)amino]pyridine
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Used as a highly effective reagent in organic synthesis, particularly as a precursor for generating electrophilic aminating agents. It plays a key role in the preparation of nitrogen-containing compounds through electrophilic amination of carbon nucleophiles. Commonly employed in the synthesis of heterocycles and functionalized amines, which are important in pharmaceutical and agrochemical industries. Its strong electron-withdrawing sulfonyl groups enhance reactivity and stability of intermediates, makin

Used as a highly effective reagent in organic synthesis, particularly as a precursor for generating electrophilic aminating agents. It plays a key role in the preparation of nitrogen-containing compounds through electrophilic amination of carbon nucleophiles. Commonly employed in the synthesis of heterocycles and functionalized amines, which are important in pharmaceutical and agrochemical industries. Its strong electron-withdrawing sulfonyl groups enhance reactivity and stability of intermediates, making it valuable in transition metal-catalyzed reactions and modern C–H functionalization processes.

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