1-(tert-Butyldimethylsilyloxy)-1-methoxyethene
95%
- Product Code: 88137
CAS:
77086-38-5
Molecular Weight: | 188.34 g./mol | Molecular Formula: | C₉H₂₀O₂Si |
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EC Number: | MDL Number: | MFCD02683524 | |
Melting Point: | Boiling Point: | 62ºC9 mm Hg | |
Density: | 0.863 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used as a protective group in organic synthesis, particularly for alcohols and diols. It helps in selectively masking hydroxyl groups during multi-step reactions, ensuring that only the desired functional groups react. It is also employed in the synthesis of complex natural products and pharmaceuticals, where precise control over reactivity is crucial. Additionally, it serves as a reagent in the preparation of silyl enol ethers, which are intermediates in various carbon-carbon bond-forming reactions, such as aldol condensations. Its stability and ease of removal under mild conditions make it a valuable tool in synthetic chemistry.
Product Specification:
Test | Specification |
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APPEARANCE | Colorless to Almost colorless clear liquid |
PURITY | 94.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $141.57 |
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5.000 | 10-20 days | $550.56 |
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1-(tert-Butyldimethylsilyloxy)-1-methoxyethene
This chemical is primarily used as a protective group in organic synthesis, particularly for alcohols and diols. It helps in selectively masking hydroxyl groups during multi-step reactions, ensuring that only the desired functional groups react. It is also employed in the synthesis of complex natural products and pharmaceuticals, where precise control over reactivity is crucial. Additionally, it serves as a reagent in the preparation of silyl enol ethers, which are intermediates in various carbon-carbon bond-forming reactions, such as aldol condensations. Its stability and ease of removal under mild conditions make it a valuable tool in synthetic chemistry.
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