Allyltriethylsilane
≥95%
- Product Code: 56566
CAS:
17898-21-4
| Molecular Weight: | 156.34 g./mol | Molecular Formula: | C₉H₂₀Si |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Allyltriethylsilane is primarily used in organic synthesis as a versatile reagent for the protection of alcohols. It reacts with alcohols to form silyl ethers, which are stable under a variety of reaction conditions, allowing for selective transformations in complex molecules. This compound is particularly valuable in the synthesis of natural products and pharmaceuticals, where temporary protection of hydroxyl groups is often required. Additionally, it serves as a precursor in the preparation of silicon-containing polymers and materials, contributing to the development of advanced coatings and adhesives. Its allyl group also enables participation in various catalytic processes, such as hydrosilylation, which is useful in the production of organosilicon compounds.
Product Specification:
| Test | Specification |
|---|---|
| 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 |
|---|---|---|---|
| 1.000 | 10-20 days | ฿810.00 |
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| 5.000 | 10-20 days | ฿2,900.00 |
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Allyltriethylsilane
Allyltriethylsilane is primarily used in organic synthesis as a versatile reagent for the protection of alcohols. It reacts with alcohols to form silyl ethers, which are stable under a variety of reaction conditions, allowing for selective transformations in complex molecules. This compound is particularly valuable in the synthesis of natural products and pharmaceuticals, where temporary protection of hydroxyl groups is often required. Additionally, it serves as a precursor in the preparation of silicon-containing polymers and materials, contributing to the development of advanced coatings and adhesives. Its allyl group also enables participation in various catalytic processes, such as hydrosilylation, which is useful in the production of organosilicon compounds.
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