Tributylstannyltrimethylsilane
95%
- Product Code: 58481
CAS:
17955-46-3
| Molecular Weight: | 363.23 g./mol | Molecular Formula: | C₁₅H₃₆SiSn |
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| EC Number: | MDL Number: | MFCD00054903 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.04g/mL | Storage Condition: | room temperature, dry |
Product Description:
Tributylstannyltrimethylsilane is primarily used in organic synthesis as a reagent for the introduction of trimethylsilyl groups into molecules. It is particularly valuable in the protection of hydroxyl groups during complex chemical reactions, ensuring that these groups remain intact while other parts of the molecule undergo transformation. Additionally, it serves as a key intermediate in the preparation of organosilicon compounds, which are widely utilized in the production of silicone polymers, resins, and elastomers. Its ability to facilitate selective silylation reactions makes it a crucial component in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Furthermore, it is employed in cross-coupling reactions, enabling the formation of carbon-carbon bonds, which is essential in the development of advanced materials and bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $147.24 |
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Tributylstannyltrimethylsilane
Tributylstannyltrimethylsilane is primarily used in organic synthesis as a reagent for the introduction of trimethylsilyl groups into molecules. It is particularly valuable in the protection of hydroxyl groups during complex chemical reactions, ensuring that these groups remain intact while other parts of the molecule undergo transformation. Additionally, it serves as a key intermediate in the preparation of organosilicon compounds, which are widely utilized in the production of silicone polymers, resins, and elastomers. Its ability to facilitate selective silylation reactions makes it a crucial component in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Furthermore, it is employed in cross-coupling reactions, enabling the formation of carbon-carbon bonds, which is essential in the development of advanced materials and bioactive molecules.
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