2-Bromoethyl trifluoromethanesulfonate
≥95%
- Product Code: 79653
CAS:
103935-47-3
| Molecular Weight: | 257.03 g./mol | Molecular Formula: | C₃H₄BrF₃O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11656439 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily used as an alkylating agent in organic synthesis, particularly for introducing the trifluoromethanesulfonate (triflate) group into molecules. It is valuable in the preparation of complex organic compounds, including pharmaceuticals and agrochemicals, due to its ability to act as a reactive intermediate.
In medicinal chemistry, it is employed to modify or functionalize molecules, enhancing their biological activity or stability. Additionally, it is utilized in the synthesis of polymers and materials where the triflate group can improve properties such as thermal stability or chemical resistance. Its reactivity makes it a useful tool in cross-coupling reactions and other advanced synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,683.00 |
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| 0.250 | 10-20 days | ฿2,529.00 |
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| 1.000 | 10-20 days | ฿5,688.00 |
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| 5.000 | 10-20 days | ฿22,743.00 |
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2-Bromoethyl trifluoromethanesulfonate
This chemical is primarily used as an alkylating agent in organic synthesis, particularly for introducing the trifluoromethanesulfonate (triflate) group into molecules. It is valuable in the preparation of complex organic compounds, including pharmaceuticals and agrochemicals, due to its ability to act as a reactive intermediate.
In medicinal chemistry, it is employed to modify or functionalize molecules, enhancing their biological activity or stability. Additionally, it is utilized in the synthesis of polymers and materials where the triflate group can improve properties such as thermal stability or chemical resistance. Its reactivity makes it a useful tool in cross-coupling reactions and other advanced synthetic methodologies.
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