Trimethylsilyl azide
93%
- Product Code: 60061
Alias:
Azidotrimethylsilane ; trimethylsilane azide, trimethylsilyl azide compound, trimethyl silicon azide, azidotrimethylsilane, trimethyl azidosilane
CAS:
4648-54-8
Molecular Weight: | 115.21 g./mol | Molecular Formula: | C₃H₉N₃Si |
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EC Number: | 225-078-5 | MDL Number: | MFCD00001986 |
Melting Point: | -95°C | Boiling Point: | 52-53 °C/175 mmHg(lit.) |
Density: | 0.868 g/mL at 25 °C(lit.) | Storage Condition: | 2~8℃, dry, sealed |
Product Description:
Trimethylsilyl azide is widely used in organic synthesis as a reagent for introducing the azide functional group into molecules. It is particularly valuable in the preparation of azido compounds, which serve as intermediates in the synthesis of various pharmaceuticals, agrochemicals, and polymers. The compound is often employed in click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC), to create triazole derivatives. These derivatives are important in drug discovery and materials science due to their stability and biological activity. Additionally, trimethylsilyl azide is utilized in the synthesis of heterocycles and in the modification of peptides and proteins, enhancing their functional properties. Its ability to act as a protecting group for alcohols and amines further extends its utility in complex organic transformations.
Product Specification:
Test | Specification |
---|---|
PurityGC | 93 100% |
REFRACTIVE INDEX N20D | 1.413-1.417 |
APPEARANCE | Colorless to light yellow liquid |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | Ft3,770.94 |
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5.000 | 10-20 days | Ft4,848.35 |
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25.000 | 10-20 days | Ft19,824.36 |
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100.000 | 10-20 days | Ft55,594.40 |
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500.000 | 10-20 days | Ft266,012.73 |
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Trimethylsilyl azide
Trimethylsilyl azide is widely used in organic synthesis as a reagent for introducing the azide functional group into molecules. It is particularly valuable in the preparation of azido compounds, which serve as intermediates in the synthesis of various pharmaceuticals, agrochemicals, and polymers. The compound is often employed in click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC), to create triazole derivatives. These derivatives are important in drug discovery and materials science due to their stability and biological activity. Additionally, trimethylsilyl azide is utilized in the synthesis of heterocycles and in the modification of peptides and proteins, enhancing their functional properties. Its ability to act as a protecting group for alcohols and amines further extends its utility in complex organic transformations.
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