2-(Triisopropylsilyl)-5-(trimethylstannyl)thiazole
98%
- Product Code: 62184
CAS:
1005196-16-6
| Molecular Weight: | 404.27 g./mol | Molecular Formula: | C₁₅H₃₁NSSiSn |
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| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the construction of complex molecules. Its triisopropylsilyl group serves as a protective moiety for sensitive functional groups, allowing selective reactions to occur without interference. The trimethylstannyl moiety is highly reactive in cross-coupling reactions, such as the Stille coupling, enabling the formation of carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its thiazole ring is a key structural motif in many biologically active compounds, making it valuable in medicinal chemistry for developing drugs targeting various diseases. Additionally, its unique structure is explored in materials science for creating specialized polymers or conductive materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $144.65 |
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2-(Triisopropylsilyl)-5-(trimethylstannyl)thiazole
This compound is primarily utilized in organic synthesis, particularly in the construction of complex molecules. Its triisopropylsilyl group serves as a protective moiety for sensitive functional groups, allowing selective reactions to occur without interference. The trimethylstannyl moiety is highly reactive in cross-coupling reactions, such as the Stille coupling, enabling the formation of carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its thiazole ring is a key structural motif in many biologically active compounds, making it valuable in medicinal chemistry for developing drugs targeting various diseases. Additionally, its unique structure is explored in materials science for creating specialized polymers or conductive materials.
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