N-(5-Chloro-2-pyridyl)bis(trifluoromethanesulfonimide)

98%

Reagent Code: #72751
label
Alias N-(5-Chloro-2-pyridyl)bis(trifluoromethanesulfonylimide)2-[N,N-bis(trifluoromethylsulfonyl)amino]-5-chloropyridineN,N-bis (Trifluoromethylsulfonyl)-5-chloro-2-pyridinamine
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CAS Number 145100-51-2

science Other reagents with same CAS 145100-51-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 392.68 g/mol
Formula C₇H₃ClF₆N₂O₄S₂
badge Registry Numbers
MDL Number MFCD00191833
thermostat Physical Properties
Melting Point 45-47 °C(lit.)
Boiling Point 77-90°C/0.2mmHg
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used as a reagent in organic synthesis, particularly for introducing the trifluoromethanesulfonyl (triflyl) group into molecules. It is highly effective in the preparation of triflyl derivatives, which are valuable intermediates in the development of pharmaceuticals, agrochemicals, and advanced materials. The compound is also employed in catalytic reactions, where it acts as a strong electrophile, facilitating the formation of carbon-nitrogen and carbon-carbon bonds. Its stability and reactivity make it a preferred choice in the synthesis of complex organic compounds, especially in the field of medicinal chemistry where triflyl groups enhance the biological activity of molecules.

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Test Parameter Specification
Purity 97.5-100%
Appearance White to Orange to Tan Solid
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure
Note Low melting point solid; may change state in different environments (solid, liquid or semi-solid)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,020.00
inventory 1g
10-20 days ฿300.00

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N-(5-Chloro-2-pyridyl)bis(trifluoromethanesulfonimide)
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This chemical is primarily used as a reagent in organic synthesis, particularly for introducing the trifluoromethanesulfonyl (triflyl) group into molecules. It is highly effective in the preparation of triflyl derivatives, which are valuable intermediates in the development of pharmaceuticals, agrochemicals, and advanced materials. The compound is also employed in catalytic reactions, where it acts as a strong electrophile, facilitating the formation of carbon-nitrogen and carbon-carbon bonds. Its stabil

This chemical is primarily used as a reagent in organic synthesis, particularly for introducing the trifluoromethanesulfonyl (triflyl) group into molecules. It is highly effective in the preparation of triflyl derivatives, which are valuable intermediates in the development of pharmaceuticals, agrochemicals, and advanced materials. The compound is also employed in catalytic reactions, where it acts as a strong electrophile, facilitating the formation of carbon-nitrogen and carbon-carbon bonds. Its stability and reactivity make it a preferred choice in the synthesis of complex organic compounds, especially in the field of medicinal chemistry where triflyl groups enhance the biological activity of molecules.

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