(S)-tert-Butyl (1-((tert-butyldimethylsilyl)oxy)-3-hydroxypropan-2-yl)carbamate
≥95%
- Product Code: 37797
CAS:
185692-85-7
| Molecular Weight: | 305.49 g./mol | Molecular Formula: | C₁₄H₃₁NO₄Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28403204 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as a protected intermediate for the preparation of complex molecules, particularly in pharmaceutical research. Its structure, featuring both tert-butyl and tert-butyldimethylsilyl protecting groups, makes it valuable for selective deprotection strategies during multi-step syntheses. It is often employed in the development of peptides, amino acid derivatives, and other bioactive compounds where controlled reactivity and stability are essential. Additionally, its chiral center allows for stereoselective synthesis, making it useful in the production of enantiomerically pure substances. Its applications are particularly relevant in medicinal chemistry for designing drug candidates with specific biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,059.00 |
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| 0.250 | 10-20 days | ฿6,525.00 |
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| 1.000 | 10-20 days | ฿16,380.00 |
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(S)-tert-Butyl (1-((tert-butyldimethylsilyl)oxy)-3-hydroxypropan-2-yl)carbamate
This chemical is primarily utilized in organic synthesis as a protected intermediate for the preparation of complex molecules, particularly in pharmaceutical research. Its structure, featuring both tert-butyl and tert-butyldimethylsilyl protecting groups, makes it valuable for selective deprotection strategies during multi-step syntheses. It is often employed in the development of peptides, amino acid derivatives, and other bioactive compounds where controlled reactivity and stability are essential. Additionally, its chiral center allows for stereoselective synthesis, making it useful in the production of enantiomerically pure substances. Its applications are particularly relevant in medicinal chemistry for designing drug candidates with specific biological activities.
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