Fluorotrimethylsilylketene Ethyl Trimethylsilyl Acetal (mixture of isomers)
≥95%(GC)
- Product Code: 82744
CAS:
1068142-02-8
| Molecular Weight: | 250.46 g./mol | Molecular Formula: | C₁₀H₂₃FO₂Si₂ |
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| Density: | 0.92 | Storage Condition: | 2-8°C |
Product Description:
Fluorotrimethylsilylketene Ethyl Trimethylsilyl Acetal is primarily utilized in organic synthesis as a versatile reagent for introducing functional groups into complex molecules. Its unique structure allows it to participate in various reactions, such as cycloadditions and nucleophilic additions, making it valuable in the construction of cyclic and acyclic compounds. This chemical is particularly useful in the development of pharmaceuticals, where it aids in the synthesis of active pharmaceutical ingredients (APIs) with specific stereochemistry. Additionally, it finds application in the preparation of advanced materials, including polymers and specialty chemicals, due to its ability to modify molecular frameworks efficiently. Its reactivity with silyl groups also makes it a key component in protecting group chemistry, enabling selective transformations in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿9,693.00 |
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| 5.000 | 10-20 days | ฿19,413.00 |
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Fluorotrimethylsilylketene Ethyl Trimethylsilyl Acetal (mixture of isomers)
Fluorotrimethylsilylketene Ethyl Trimethylsilyl Acetal is primarily utilized in organic synthesis as a versatile reagent for introducing functional groups into complex molecules. Its unique structure allows it to participate in various reactions, such as cycloadditions and nucleophilic additions, making it valuable in the construction of cyclic and acyclic compounds. This chemical is particularly useful in the development of pharmaceuticals, where it aids in the synthesis of active pharmaceutical ingredients (APIs) with specific stereochemistry. Additionally, it finds application in the preparation of advanced materials, including polymers and specialty chemicals, due to its ability to modify molecular frameworks efficiently. Its reactivity with silyl groups also makes it a key component in protecting group chemistry, enabling selective transformations in multi-step synthetic processes.
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