Sodium bis(trimethylsilyl)amide
1.0 M solution in THF,MKSeal
- Product Code: 67805
CAS:
1070-89-9
Molecular Weight: | 183.37 g./mol | Molecular Formula: | C₆H₁₈NNaSi₂ |
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EC Number: | 213-983-8 | MDL Number: | MFCD00009835 |
Melting Point: | 171-175 °C(lit.) | Boiling Point: | 67°C |
Density: | 0.904 g/mL at 25 °C | Storage Condition: | 2~8 ℃ |
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.
Product Specification:
Test | Specification |
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APPEARANCE | Light yellow to brown liquid |
Purity Titration by HCl | 0.95M 1.10M |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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100.000 | 10-20 days | ฿1,850.00 |
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500.000 | 10-20 days | ฿4,450.00 |
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800.000 | 10-20 days | ฿5,970.00 |
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1000.000 | 10-20 days | ฿6,560.00 |
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Sodium bis(trimethylsilyl)amide
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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