2,6-DiMethoxyphenyl trifluoroMethanesulfonate
97%
- Product Code: 41029
CAS:
60319-07-5
| Molecular Weight: | 286.23 g./mol | Molecular Formula: | C₉H₉F₃O₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06411304 | |
| Melting Point: | Boiling Point: | 115℃/0.2 mmHg (lit.) | |
| Density: | 1.376 g/mL at 25℃ (lit.) | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily used in organic synthesis as a versatile reagent for introducing the 2,6-dimethoxyphenyl group into various molecular structures. It is particularly valuable in the preparation of complex organic compounds, including pharmaceuticals and agrochemicals, where the 2,6-dimethoxyphenyl moiety can enhance biological activity or stability. Additionally, it serves as a key intermediate in the synthesis of advanced materials, such as polymers and ligands for catalysis, due to its ability to act as a protective group or a reactive site for further functionalization. Its trifluoromethanesulfonate group also makes it a useful leaving group in nucleophilic substitution reactions, enabling efficient bond formation in synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $210.49 |
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2,6-DiMethoxyphenyl trifluoroMethanesulfonate
This chemical is primarily used in organic synthesis as a versatile reagent for introducing the 2,6-dimethoxyphenyl group into various molecular structures. It is particularly valuable in the preparation of complex organic compounds, including pharmaceuticals and agrochemicals, where the 2,6-dimethoxyphenyl moiety can enhance biological activity or stability. Additionally, it serves as a key intermediate in the synthesis of advanced materials, such as polymers and ligands for catalysis, due to its ability to act as a protective group or a reactive site for further functionalization. Its trifluoromethanesulfonate group also makes it a useful leaving group in nucleophilic substitution reactions, enabling efficient bond formation in synthetic pathways.
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