bistrifluoromethanesulfonimidate

Aquatic grade, 99.99% trace metals basis

Reagent Code: #141924
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Alias Lithium bistrifluoromethanesulfonimide
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CAS Number 90076-65-6

science Other reagents with same CAS 90076-65-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.09 g/mol
Formula C₂F₆LiNO₄S₂
badge Registry Numbers
EC Number 415-300-0
MDL Number MFCD00210017
thermostat Physical Properties
Melting Point 234-238 °C(lit.)
inventory_2 Storage & Handling
Density 1.334 g/cm3
Storage Room temperature, dry

description Product Description

Used as a highly effective reagent in organic synthesis, particularly for introducing the triflimide group into molecules. It plays a key role in the preparation of triflimide salts, which are strong, thermally stable acids used as catalysts in various reactions. Commonly employed in the synthesis of pharmaceuticals and agrochemicals due to its ability to enhance reaction efficiency and selectivity. Also utilized in materials science for modifying electronic properties of compounds, especially in the development of ionic liquids and electrolytes for advanced battery systems. Its high leaving group ability makes it valuable in cross-coupling reactions and transition-metal-catalyzed transformations.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Powder
Purity (Based on Trace Metal Analysis) (%) 99.99-100%
Water (ppm) 0-250
Trace Metal Analysis (ppm) 0-150.0
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure
ICP Major Analysis Confirms Lithium Component

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿5,080.00
inventory 25g
10-20 days ฿15,250.00
inventory 100g
10-20 days ฿38,100.00
inventory 500g
10-20 days ฿114,400.00

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bistrifluoromethanesulfonimidate
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Used as a highly effective reagent in organic synthesis, particularly for introducing the triflimide group into molecules. It plays a key role in the preparation of triflimide salts, which are strong, thermally stable acids used as catalysts in various reactions. Commonly employed in the synthesis of pharmaceuticals and agrochemicals due to its ability to enhance reaction efficiency and selectivity. Also utilized in materials science for modifying electronic properties of compounds, especially in the dev

Used as a highly effective reagent in organic synthesis, particularly for introducing the triflimide group into molecules. It plays a key role in the preparation of triflimide salts, which are strong, thermally stable acids used as catalysts in various reactions. Commonly employed in the synthesis of pharmaceuticals and agrochemicals due to its ability to enhance reaction efficiency and selectivity. Also utilized in materials science for modifying electronic properties of compounds, especially in the development of ionic liquids and electrolytes for advanced battery systems. Its high leaving group ability makes it valuable in cross-coupling reactions and transition-metal-catalyzed transformations.

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