4-Nitrophenyl Trifluoromethanesulfonate
≥99%
- Product Code: 121857
CAS:
17763-80-3
| Molecular Weight: | 271.17 g./mol | Molecular Formula: | C₇H₄F₃NO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00192354 | |
| Melting Point: | 52-56°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
4-Nitrophenyl Trifluoromethanesulfonate is widely used as a reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It serves as an effective triflating agent, enabling the introduction of the trifluoromethanesulfonate (triflate) group into organic molecules, which enhances their reactivity in subsequent reactions. This compound is especially valuable in the synthesis of complex molecules, including pharmaceuticals and agrochemicals, where it facilitates the creation of intermediates with high selectivity and efficiency. Additionally, it is employed in cross-coupling reactions, such as Suzuki and Heck couplings, to generate aryl triflates, which are pivotal in constructing diverse aromatic compounds. Its stability and reactivity make it a preferred choice in advanced chemical research and industrial applications.
Product Specification:
| Test | Specification |
|---|---|
| Purity (%) | 99-100 |
| Water | |
| Nmr Conforms To Structure | Conforms to Structure |
| Appearance | Slightly Pale Yellow To Yellow Crystal Or Powder |
| Melting Point (Degree Celsius) | 52-56 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿680.00 |
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| 5.000 | 10-20 days | ฿2,580.00 |
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| 25.000 | 10-20 days | ฿8,620.00 |
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4-Nitrophenyl Trifluoromethanesulfonate
4-Nitrophenyl Trifluoromethanesulfonate is widely used as a reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It serves as an effective triflating agent, enabling the introduction of the trifluoromethanesulfonate (triflate) group into organic molecules, which enhances their reactivity in subsequent reactions. This compound is especially valuable in the synthesis of complex molecules, including pharmaceuticals and agrochemicals, where it facilitates the creation of intermediates with high selectivity and efficiency. Additionally, it is employed in cross-coupling reactions, such as Suzuki and Heck couplings, to generate aryl triflates, which are pivotal in constructing diverse aromatic compounds. Its stability and reactivity make it a preferred choice in advanced chemical research and industrial applications.
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