1-Methyl-5-(tributylstannyl)-3-(trifluoromethyl)-1H-pyrazole
95%
- Product Code: 88823
CAS:
191606-78-7
| Molecular Weight: | 439.138 g./mol | Molecular Formula: | C₁₇H₃₁F₃N₂Sn |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06797466 | |
| Melting Point: | Boiling Point: | 396.4ºC at 760mmHg | |
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate for the construction of complex molecules. Its tributylstannyl group makes it valuable in Stille coupling reactions, enabling the formation of carbon-carbon bonds in the presence of palladium catalysts. This is especially useful in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl group enhances the compound's reactivity and stability, making it suitable for applications in medicinal chemistry, where fluorine-containing compounds are often sought after for their unique properties. Additionally, it can be employed in the development of pyrazole derivatives, which are known for their biological activities, including anti-inflammatory, antimicrobial, and anticancer effects. Its role in fine chemical production underscores its importance in research and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿7,200.00 |
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| 1.000 | 10-20 days | ฿15,750.00 |
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| 5.000 | 10-20 days | ฿61,200.00 |
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1-Methyl-5-(tributylstannyl)-3-(trifluoromethyl)-1H-pyrazole
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate for the construction of complex molecules. Its tributylstannyl group makes it valuable in Stille coupling reactions, enabling the formation of carbon-carbon bonds in the presence of palladium catalysts. This is especially useful in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl group enhances the compound's reactivity and stability, making it suitable for applications in medicinal chemistry, where fluorine-containing compounds are often sought after for their unique properties. Additionally, it can be employed in the development of pyrazole derivatives, which are known for their biological activities, including anti-inflammatory, antimicrobial, and anticancer effects. Its role in fine chemical production underscores its importance in research and industrial processes.
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