Ethyl 4-((tert-butyldimethylsilyl)oxy)-3-oxobutanoate
95%
- Product Code: 83762
CAS:
1341195-54-7
| Molecular Weight: | 260.40 g./mol | Molecular Formula: | C₁₂H₂₄O₄Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11975818 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily used in organic synthesis as a protected form of a β-keto ester. The tert-butyldimethylsilyl (TBDMS) group serves as a protecting group for the hydroxyl functionality, allowing selective reactions to occur at other sites of the molecule without interference. It is particularly valuable in the synthesis of complex organic molecules, such as pharmaceuticals and natural products, where precise control over reactivity is essential. The β-keto ester moiety is a versatile intermediate, enabling further transformations like alkylation, reduction, or cyclization reactions. This compound is often employed in multi-step synthetic routes to construct key structural motifs in target molecules. Its stability and ease of deprotection make it a useful tool in modern synthetic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | liquid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,980.00 |
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| 0.250 | 10-20 days | ฿17,100.00 |
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| 1.000 | 10-20 days | ฿46,188.00 |
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Ethyl 4-((tert-butyldimethylsilyl)oxy)-3-oxobutanoate
This compound is primarily used in organic synthesis as a protected form of a β-keto ester. The tert-butyldimethylsilyl (TBDMS) group serves as a protecting group for the hydroxyl functionality, allowing selective reactions to occur at other sites of the molecule without interference. It is particularly valuable in the synthesis of complex organic molecules, such as pharmaceuticals and natural products, where precise control over reactivity is essential. The β-keto ester moiety is a versatile intermediate, enabling further transformations like alkylation, reduction, or cyclization reactions. This compound is often employed in multi-step synthetic routes to construct key structural motifs in target molecules. Its stability and ease of deprotection make it a useful tool in modern synthetic chemistry.
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