6-Methoxy-3,4-dihydronaphthalen-1-yl trifluoromethanesulfonate
95%
- Product Code: 61484
CAS:
115375-59-2
| Molecular Weight: | 308.27 g./mol | Molecular Formula: | C₁₂H₁₁F₃O₄S |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecular structures. Its trifluoromethanesulfonate group acts as a highly reactive leaving group, enabling efficient participation in cross-coupling reactions, such as Suzuki or Heck reactions, to form carbon-carbon bonds. The methoxy and dihydronaphthalene moieties make it particularly useful in the synthesis of pharmacologically active compounds, including potential drug candidates targeting neurological or cardiovascular diseases. Additionally, it serves as a precursor in the development of advanced materials, such as liquid crystals or organic semiconductors, due to its aromatic and electron-donating properties. Its stability and reactivity under mild conditions 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 | ฿2,322.00 |
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| 0.250 | 10-20 days | ฿3,474.00 |
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| 1.000 | 10-20 days | ฿8,640.00 |
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6-Methoxy-3,4-dihydronaphthalen-1-yl trifluoromethanesulfonate
This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecular structures. Its trifluoromethanesulfonate group acts as a highly reactive leaving group, enabling efficient participation in cross-coupling reactions, such as Suzuki or Heck reactions, to form carbon-carbon bonds. The methoxy and dihydronaphthalene moieties make it particularly useful in the synthesis of pharmacologically active compounds, including potential drug candidates targeting neurological or cardiovascular diseases. Additionally, it serves as a precursor in the development of advanced materials, such as liquid crystals or organic semiconductors, due to its aromatic and electron-donating properties. Its stability and reactivity under mild conditions make it a valuable tool in both academic research and industrial applications.
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