Methyl 5-oxo-7-(((trifluoromethyl)sulfonyl)oxy)-1,2,3,5-tetrahydroindolizine-3-carboxylate
95%
- Product Code: 84084
CAS:
1956310-54-5
Molecular Weight: | 341.26 g./mol | Molecular Formula: | C₁₁H₁₀F₃NO₆S |
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EC Number: | MDL Number: | MFCD29917088 | |
Melting Point: | Boiling Point: | 431.1±45.0 °C(Predicted) | |
Density: | 1.63±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly as an intermediate in the development of complex molecules. Its structure, featuring a trifluoromethylsulfonyloxy group, makes it a valuable precursor in the synthesis of biologically active compounds, including pharmaceuticals and agrochemicals. It is often employed in reactions where the introduction of the trifluoromethyl group is necessary, as this moiety can enhance the metabolic stability and bioavailability of the final product. Additionally, its reactive sites allow for further functionalization, enabling the creation of diverse chemical entities for research and industrial applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿5,058.00 |
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0.250 | 10-20 days | ฿11,691.00 |
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1.000 | 10-20 days | ฿29,160.00 |
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Methyl 5-oxo-7-(((trifluoromethyl)sulfonyl)oxy)-1,2,3,5-tetrahydroindolizine-3-carboxylate
This chemical is primarily utilized in organic synthesis, particularly as an intermediate in the development of complex molecules. Its structure, featuring a trifluoromethylsulfonyloxy group, makes it a valuable precursor in the synthesis of biologically active compounds, including pharmaceuticals and agrochemicals. It is often employed in reactions where the introduction of the trifluoromethyl group is necessary, as this moiety can enhance the metabolic stability and bioavailability of the final product. Additionally, its reactive sites allow for further functionalization, enabling the creation of diverse chemical entities for research and industrial applications.
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