(2-Azidoethoxy)(tert-butyl)dimethylsilane
≥95%
- Product Code: 68992
CAS:
113274-21-8
| Molecular Weight: | 201.34 g./mol | Molecular Formula: | C₈H₁₉N₃OSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22423155 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the protection of hydroxyl groups during complex chemical reactions. The tert-butyldimethylsilyl (TBDMS) group serves as a protecting group for alcohols, ensuring they remain unreactive while other parts of the molecule undergo transformations. The azido group introduces azide functionality, which is valuable in click chemistry applications, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction. This makes it a useful reagent in the synthesis of pharmaceuticals, bioconjugates, and materials science, where selective and efficient chemical modifications are required. Its stability and reactivity profile make it suitable for constructing complex molecular architectures in a controlled manner.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to yellow liquid |
| PURITY | 95-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿11,620.00 |
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| 5.000 | 10-20 days | ฿30,980.00 |
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(2-Azidoethoxy)(tert-butyl)dimethylsilane
This chemical is primarily used in organic synthesis, particularly in the protection of hydroxyl groups during complex chemical reactions. The tert-butyldimethylsilyl (TBDMS) group serves as a protecting group for alcohols, ensuring they remain unreactive while other parts of the molecule undergo transformations. The azido group introduces azide functionality, which is valuable in click chemistry applications, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction. This makes it a useful reagent in the synthesis of pharmaceuticals, bioconjugates, and materials science, where selective and efficient chemical modifications are required. Its stability and reactivity profile make it suitable for constructing complex molecular architectures in a controlled manner.
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