tert-Butyl 3-amino-3-(trifluoromethyl)azetidine-1-carboxylate
95%
- Product Code: 124175
CAS:
1258652-24-2
| Molecular Weight: | 240.22 g./mol | Molecular Formula: | C₉H₁₅F₃N₂O₂ |
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| EC Number: | MDL Number: | MFCD17480497 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry, protected from light |
Product Description:
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical industry. It plays a key role in the development of active pharmaceutical ingredients (APIs) due to its trifluoromethyl and azetidine groups, which are valuable in drug design for enhancing metabolic stability and bioavailability. It is also utilized in the preparation of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, its tert-butyl carboxylate group provides a protective function during synthetic processes, allowing for selective reactions in multi-step syntheses. Its application extends to research and development in medicinal chemistry, where it contributes to the exploration of novel drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft183,267.58 |
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| 0.250 | 10-20 days | Ft402,412.93 |
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tert-Butyl 3-amino-3-(trifluoromethyl)azetidine-1-carboxylate
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical industry. It plays a key role in the development of active pharmaceutical ingredients (APIs) due to its trifluoromethyl and azetidine groups, which are valuable in drug design for enhancing metabolic stability and bioavailability. It is also utilized in the preparation of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, its tert-butyl carboxylate group provides a protective function during synthetic processes, allowing for selective reactions in multi-step syntheses. Its application extends to research and development in medicinal chemistry, where it contributes to the exploration of novel drug candidates.
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