3-((tert-Butyldimethylsilyl)oxy)cyclobutanone
98%
- Product Code: 153701
CAS:
929913-18-8
| Molecular Weight: | 200.353 g./mol | Molecular Formula: | C₁₀H₂₀O₂Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23105928 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, dry |
Product Description:
Used primarily as a protected hydroxyketone intermediate in organic synthesis, particularly in the construction of complex natural products and pharmaceuticals. The silyl ether group provides stability and selectivity during multi-step reactions, allowing for controlled transformations at other reactive sites. Commonly employed in stereoselective reductions, nucleophilic additions, and ring-forming reactions where protection of the alcohol functionality is required. Its cyclobutanone core serves as a strained ring system useful in ring-expansion or fragmentation strategies. Widely utilized in medicinal chemistry for the synthesis of bioactive molecules where temporary protection of polar groups is needed to improve solubility or reactivity in non-aqueous environments.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,610.00 |
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| 0.250 | 10-20 days | ฿12,370.00 |
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| 1.000 | 10-20 days | ฿22,680.00 |
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| 5.000 | 10-20 days | ฿91,480.00 |
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3-((tert-Butyldimethylsilyl)oxy)cyclobutanone
Used primarily as a protected hydroxyketone intermediate in organic synthesis, particularly in the construction of complex natural products and pharmaceuticals. The silyl ether group provides stability and selectivity during multi-step reactions, allowing for controlled transformations at other reactive sites. Commonly employed in stereoselective reductions, nucleophilic additions, and ring-forming reactions where protection of the alcohol functionality is required. Its cyclobutanone core serves as a strained ring system useful in ring-expansion or fragmentation strategies. Widely utilized in medicinal chemistry for the synthesis of bioactive molecules where temporary protection of polar groups is needed to improve solubility or reactivity in non-aqueous environments.
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