(S)-ethyl 2-((tert-butoxycarbonyl)amino)-3-(4-(((trifluoromethyl)sulfonyl)oxy)phenyl)propanoate
95%
- Product Code: 82992
CAS:
169158-01-4
| Molecular Weight: | 441.42 g./mol | Molecular Formula: | C₁₇H₂₂F₃NO₇S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30472153 | |
| Melting Point: | Boiling Point: | 508.1±50.0 °C(Predicted) | |
| Density: | 1.329±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its structure, featuring a trifluoromethylsulfonyloxy group, makes it valuable for introducing trifluoromethylated aromatic compounds, which are often found in drugs due to their enhanced metabolic stability and bioavailability. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions in multi-step synthetic processes, enabling the creation of highly specific and potent therapeutic agents. Its application is crucial in the development of drugs for conditions such as cancer, inflammation, and central nervous system disorders.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,360.00 |
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| 0.250 | 10-20 days | ฿17,550.00 |
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| 1.000 | 10-20 days | ฿35,100.00 |
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(S)-ethyl 2-((tert-butoxycarbonyl)amino)-3-(4-(((trifluoromethyl)sulfonyl)oxy)phenyl)propanoate
This chemical is primarily used in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its structure, featuring a trifluoromethylsulfonyloxy group, makes it valuable for introducing trifluoromethylated aromatic compounds, which are often found in drugs due to their enhanced metabolic stability and bioavailability. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions in multi-step synthetic processes, enabling the creation of highly specific and potent therapeutic agents. Its application is crucial in the development of drugs for conditions such as cancer, inflammation, and central nervous system disorders.
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