tributyl(2-methylprop-2-enyl)stannane
≥95%
- Product Code: 88846
CAS:
67883-62-9
| Molecular Weight: | 345.14 g./mol | Molecular Formula: | C₁₆H₃₄Sn |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03425867 | |
| Melting Point: | Boiling Point: | 328.6°C | |
| Density: | 1.487 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in organic synthesis as a reagent for introducing the tributylstannyl group into organic molecules. It is particularly valuable in Stille coupling reactions, which are widely employed in the synthesis of complex organic compounds, including pharmaceuticals, natural products, and polymers. The compound facilitates the formation of carbon-carbon bonds, making it essential in the construction of intricate molecular structures. Additionally, it is utilized in the preparation of organotin compounds, which have applications in materials science, such as stabilizers in PVC production and catalysts in various chemical processes. Its role in cross-coupling reactions also extends to the development of advanced materials and electronic components.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | LIQUID |
| PURITY | 94.5-100 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $226.82 |
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tributyl(2-methylprop-2-enyl)stannane
This chemical is primarily used in organic synthesis as a reagent for introducing the tributylstannyl group into organic molecules. It is particularly valuable in Stille coupling reactions, which are widely employed in the synthesis of complex organic compounds, including pharmaceuticals, natural products, and polymers. The compound facilitates the formation of carbon-carbon bonds, making it essential in the construction of intricate molecular structures. Additionally, it is utilized in the preparation of organotin compounds, which have applications in materials science, such as stabilizers in PVC production and catalysts in various chemical processes. Its role in cross-coupling reactions also extends to the development of advanced materials and electronic components.
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