Sodium bis(trimethylsilyl)amide

1.0 M solution in THF,MKSeal

Reagent Code: #67805
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CAS Number 1070-89-9

science Other reagents with same CAS 1070-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.37 g/mol
Formula C₆H₁₈NNaSi₂
badge Registry Numbers
EC Number 213-983-8
MDL Number MFCD00009835
thermostat Physical Properties
Melting Point 171-175 °C(lit.)
Boiling Point 67°C
inventory_2 Storage & Handling
Density 0.904 g/mL at 25 °C
Storage 2~8 ℃

description Product Description

Sodium bis(trimethylsilyl)amide is widely used as a strong, non-nucleophilic base in organic synthesis. It is particularly effective in deprotonating weakly acidic compounds, such as esters, ketones, and amides, to generate reactive intermediates. This chemical is commonly employed in the preparation of enolates, which are essential for aldol condensation reactions and other carbon-carbon bond-forming processes. Additionally, it serves as a key reagent in the synthesis of organometallic compounds, where it facilitates the removal of protons to form metal-organic complexes. Its application extends to the field of polymer chemistry, where it is used to initiate anionic polymerization of certain monomers. Furthermore, it is utilized in the production of pharmaceuticals and fine chemicals, often playing a critical role in the formation of complex molecular structures.

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Test Parameter Specification
Appearance Light yellow to brown liquid
Purity (Titration by HCl) 0.95-1.10 M

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1L
10-20 days ฿6,560.00
inventory 100ml
10-20 days ฿1,850.00
inventory 500ml
10-20 days ฿4,450.00
inventory 800ml
10-20 days ฿5,970.00

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Sodium bis(trimethylsilyl)amide
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Sodium bis(trimethylsilyl)amide is widely used as a strong, non-nucleophilic base in organic synthesis. It is particularly effective in deprotonating weakly acidic compounds, such as esters, ketones, and amides, to generate reactive intermediates. This chemical is commonly employed in the preparation of enolates, which are essential for aldol condensation reactions and other carbon-carbon bond-forming processes. Additionally, it serves as a key reagent in the synthesis of organometallic compounds, where

Sodium bis(trimethylsilyl)amide is widely used as a strong, non-nucleophilic base in organic synthesis. It is particularly effective in deprotonating weakly acidic compounds, such as esters, ketones, and amides, to generate reactive intermediates. This chemical is commonly employed in the preparation of enolates, which are essential for aldol condensation reactions and other carbon-carbon bond-forming processes. Additionally, it serves as a key reagent in the synthesis of organometallic compounds, where it facilitates the removal of protons to form metal-organic complexes. Its application extends to the field of polymer chemistry, where it is used to initiate anionic polymerization of certain monomers. Furthermore, it is utilized in the production of pharmaceuticals and fine chemicals, often playing a critical role in the formation of complex molecular structures.

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