But-3-yn-1-yl trifluoromethanesulfonate
95%
- Product Code: 141385
CAS:
32264-79-2
| Molecular Weight: | 202.15 g./mol | Molecular Formula: | C₅H₅F₃O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28990060 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, Inert Gas |
Product Description:
Used primarily as an alkylating agent in organic synthesis, enabling the introduction of the but-3-yn-1-yl group to various nucleophiles. Its triflate functionality makes it highly reactive in palladium-catalyzed cross-coupling reactions, such as Sonogashira and Heck couplings, facilitating the construction of complex molecular architectures. Commonly employed in the synthesis of conjugated enynes and natural products, it serves as a versatile building block in pharmaceutical and agrochemical research. Due to the terminal alkyne moiety, it also supports click chemistry applications through copper-catalyzed azide-alkyne cycloaddition (CuAAC) after functionalization.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿13,560.00 |
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| 250mg | 10-20 days | ฿23,060.00 |
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| 1g | 10-20 days | ฿62,220.00 |
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But-3-yn-1-yl trifluoromethanesulfonate
Used primarily as an alkylating agent in organic synthesis, enabling the introduction of the but-3-yn-1-yl group to various nucleophiles. Its triflate functionality makes it highly reactive in palladium-catalyzed cross-coupling reactions, such as Sonogashira and Heck couplings, facilitating the construction of complex molecular architectures. Commonly employed in the synthesis of conjugated enynes and natural products, it serves as a versatile building block in pharmaceutical and agrochemical research. Due to the terminal alkyne moiety, it also supports click chemistry applications through copper-catalyzed azide-alkyne cycloaddition (CuAAC) after functionalization.
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