4-(Tri-n-butylstannyl)thiazole
95%
- Product Code: 58433
CAS:
173979-01-6
| Molecular Weight: | 374.17 g./mol | Molecular Formula: | C₁₅H₂₉NSSn |
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| EC Number: | MDL Number: | MFCD01319073 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It is particularly valuable in cross-coupling reactions, such as Stille coupling, where it facilitates the formation of carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stannyl group acts as a key functional group that enables efficient coupling with various electrophiles, making it a versatile reagent in the development of thiazole-containing compounds. These compounds often exhibit biological activity, making them important in drug discovery and development. Additionally, it is used in the preparation of organic semiconductors and other electronic materials due to its ability to introduce thiazole moieties, which are known for their electron-transport properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.050 | 10-20 days | €17.81 |
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| 0.250 | 10-20 days | €42.74 |
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| 1.000 | 10-20 days | €161.22 |
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4-(Tri-n-butylstannyl)thiazole
This chemical is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It is particularly valuable in cross-coupling reactions, such as Stille coupling, where it facilitates the formation of carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stannyl group acts as a key functional group that enables efficient coupling with various electrophiles, making it a versatile reagent in the development of thiazole-containing compounds. These compounds often exhibit biological activity, making them important in drug discovery and development. Additionally, it is used in the preparation of organic semiconductors and other electronic materials due to its ability to introduce thiazole moieties, which are known for their electron-transport properties.
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