3-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]-3'-trifluorobenzophenone
97%
- Product Code: 75448
CAS:
898762-05-5
| Molecular Weight: | 405.42 g./mol | Molecular Formula: | C₂₂H₂₂F₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03842209 | |
| Melting Point: | Boiling Point: | 500.1℃ at 760 mmHg | |
| Density: | 1.32g/ml | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex molecules for pharmaceutical research. Its structure, featuring a trifluorobenzophenone moiety and a dioxa-azaspirodecane group, makes it a valuable intermediate in the synthesis of compounds with potential biological activity. It is often employed in the creation of drug candidates targeting central nervous system disorders, thanks to its ability to interact with specific receptors or enzymes in the brain. Additionally, its unique spirocyclic component can enhance the stability and bioavailability of the resulting compounds, making it a key building block in medicinal chemistry. Researchers also explore its use in designing materials with specific optical or electronic properties, leveraging the trifluoromethyl group for its electron-withdrawing effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $2,413.25 |
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| 2.000 | 10-20 days | $4,009.21 |
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3-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]-3'-trifluorobenzophenone
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex molecules for pharmaceutical research. Its structure, featuring a trifluorobenzophenone moiety and a dioxa-azaspirodecane group, makes it a valuable intermediate in the synthesis of compounds with potential biological activity. It is often employed in the creation of drug candidates targeting central nervous system disorders, thanks to its ability to interact with specific receptors or enzymes in the brain. Additionally, its unique spirocyclic component can enhance the stability and bioavailability of the resulting compounds, making it a key building block in medicinal chemistry. Researchers also explore its use in designing materials with specific optical or electronic properties, leveraging the trifluoromethyl group for its electron-withdrawing effects.
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