Sodium bis(trimethylsilyl)amide
2.0 M solution in THF,MKSeal
- Product Code: 67803
Alias:
Sodium Bis(trimethylsilyl)amide; Sodium Dimethylsilylamide, Sodium Hexamethyldisilazide, Sodium Hexamethyldisilazide
CAS:
1070-89-9
| Molecular Weight: | 183.37 g./mol | Molecular Formula: | C₆H₁₈NNaSi₂ |
|---|---|---|---|
| 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 base in organic synthesis, particularly in deprotonation reactions. It is highly effective in generating carbanions from weakly acidic compounds, making it valuable in the preparation of enolates, which are intermediates in aldol reactions. It also plays a key role in the synthesis of organosilicon compounds, where it facilitates the substitution of halogens with silyl groups. Additionally, it is utilized in the production of pharmaceuticals and fine chemicals, often as a reagent in the formation of complex molecular structures. Its non-nucleophilic nature makes it suitable for reactions where nucleophilic interference must be minimized.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to brown liquid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 100.000 | 10-20 days | $72.91 |
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| 500.000 | 10-20 days | $196.22 |
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| 1000.000 | 10-20 days | $310.23 |
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Sodium bis(trimethylsilyl)amide
Sodium bis(trimethylsilyl)amide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions. It is highly effective in generating carbanions from weakly acidic compounds, making it valuable in the preparation of enolates, which are intermediates in aldol reactions. It also plays a key role in the synthesis of organosilicon compounds, where it facilitates the substitution of halogens with silyl groups. Additionally, it is utilized in the production of pharmaceuticals and fine chemicals, often as a reagent in the formation of complex molecular structures. Its non-nucleophilic nature makes it suitable for reactions where nucleophilic interference must be minimized.
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