4-Iodophenyl trifluoromethanesulfonate
95%
- Product Code: 87537
CAS:
109586-39-2
| Molecular Weight: | 352.07 g./mol | Molecular Formula: | C₇H₄F₃IO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18379773 | |
| Melting Point: | Boiling Point: | ||
| Density: | 2.035±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
4-Iodophenyl trifluoromethanesulfonate is widely used in organic synthesis as a versatile reagent, particularly in cross-coupling reactions. It serves as an effective electrophile in palladium-catalyzed processes, such as Suzuki-Miyaura and Sonogashira couplings, enabling the formation of carbon-carbon bonds. The trifluoromethanesulfonate group acts as a highly reactive leaving group, while the iodine atom can participate in further functionalization. This compound is also employed in the synthesis of complex molecules, including pharmaceuticals and agrochemicals, due to its ability to introduce aryl groups into target structures. Additionally, it is utilized in the preparation of advanced materials, such as organic semiconductors and liquid crystals, where precise aryl functionalization is required. Its reactivity and stability make it a valuable tool in both academic research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,215.00 |
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| 0.250 | 10-20 days | ฿1,611.00 |
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| 1.000 | 10-20 days | ฿4,059.00 |
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4-Iodophenyl trifluoromethanesulfonate
4-Iodophenyl trifluoromethanesulfonate is widely used in organic synthesis as a versatile reagent, particularly in cross-coupling reactions. It serves as an effective electrophile in palladium-catalyzed processes, such as Suzuki-Miyaura and Sonogashira couplings, enabling the formation of carbon-carbon bonds. The trifluoromethanesulfonate group acts as a highly reactive leaving group, while the iodine atom can participate in further functionalization. This compound is also employed in the synthesis of complex molecules, including pharmaceuticals and agrochemicals, due to its ability to introduce aryl groups into target structures. Additionally, it is utilized in the preparation of advanced materials, such as organic semiconductors and liquid crystals, where precise aryl functionalization is required. Its reactivity and stability make it a valuable tool in both academic research and industrial applications.
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