tert-Butyl (3-((tert-butyldimethylsilyl)oxy)-2-oxopropyl)carbamate
95%
- Product Code: 87998
CAS:
184429-84-3
| Molecular Weight: | 303.47 g./mol | Molecular Formula: | C₁₄H₂₉NO₄Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD24466259 | |
| Melting Point: | Boiling Point: | 347.5±27. °C(Predicted) | |
| Density: | 0.975±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily used in organic synthesis as a protecting group for amines and alcohols. Its structure allows it to temporarily shield reactive functional groups during complex chemical reactions, particularly in the synthesis of peptides, natural products, and pharmaceuticals. The tert-butyldimethylsilyl (TBDMS) group protects hydroxyl groups, while the carbamate moiety safeguards amines, enabling selective transformations in multi-step synthesis. Its stability under various reaction conditions makes it a valuable tool in medicinal chemistry and drug development, where precise control over molecular modifications is essential. After the desired reactions are completed, the protecting groups can be removed under mild conditions, restoring the original functional groups without damaging the molecule.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £42.75 |
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| 0.250 | 10-20 days | £63.71 |
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| 1.000 | 10-20 days | £127.83 |
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tert-Butyl (3-((tert-butyldimethylsilyl)oxy)-2-oxopropyl)carbamate
This chemical is primarily used in organic synthesis as a protecting group for amines and alcohols. Its structure allows it to temporarily shield reactive functional groups during complex chemical reactions, particularly in the synthesis of peptides, natural products, and pharmaceuticals. The tert-butyldimethylsilyl (TBDMS) group protects hydroxyl groups, while the carbamate moiety safeguards amines, enabling selective transformations in multi-step synthesis. Its stability under various reaction conditions makes it a valuable tool in medicinal chemistry and drug development, where precise control over molecular modifications is essential. After the desired reactions are completed, the protecting groups can be removed under mild conditions, restoring the original functional groups without damaging the molecule.
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