Catechol Bis(trifluoromethanesulfonate)
≥98%
- Product Code: 122153
CAS:
17763-91-6
| Molecular Weight: | 374.22 g./mol | Molecular Formula: | C₈H₄F₆O₆S₂ |
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| EC Number: | MDL Number: | MFCD00274274 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Catechol bis(trifluoromethanesulfonate) is primarily used as a versatile reagent in organic synthesis, particularly in the introduction of trifluoromethanesulfonate (triflate) groups. These groups are highly reactive and serve as excellent leaving groups in substitution reactions, making the compound valuable in the formation of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise functional group transformations are required. Additionally, its role in cross-coupling reactions, such as Suzuki and Heck reactions, is significant for constructing carbon-carbon bonds in the development of fine chemicals and active pharmaceutical ingredients (APIs). The compound’s stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $26.73 |
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| 1.000 | 10-20 days | $71.29 |
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Catechol Bis(trifluoromethanesulfonate)
Catechol bis(trifluoromethanesulfonate) is primarily used as a versatile reagent in organic synthesis, particularly in the introduction of trifluoromethanesulfonate (triflate) groups. These groups are highly reactive and serve as excellent leaving groups in substitution reactions, making the compound valuable in the formation of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise functional group transformations are required. Additionally, its role in cross-coupling reactions, such as Suzuki and Heck reactions, is significant for constructing carbon-carbon bonds in the development of fine chemicals and active pharmaceutical ingredients (APIs). The compound’s stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.
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