4'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]-3-trifluoromethylbenzophenone
97%
- Product Code: 75520
CAS:
898758-12-8
| Molecular Weight: | 405.42 g./mol | Molecular Formula: | C₂₂H₂₂F₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03841698 | |
| Melting Point: | Boiling Point: | 495.1℃ 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 with potential pharmaceutical applications. Its structure, featuring a benzophenone core and a spirocyclic moiety, makes it a valuable intermediate in the synthesis of compounds with biological activity. It is often employed in the creation of drug candidates targeting central nervous system disorders, as the trifluoromethyl group and the spirocyclic structure can enhance binding affinity and metabolic stability. Additionally, it serves as a key building block in the preparation of ligands for receptor studies, aiding in the exploration of biochemical pathways and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿58,110.00 |
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| 2.000 | 10-20 days | ฿96,540.00 |
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4'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]-3-trifluoromethylbenzophenone
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex molecules with potential pharmaceutical applications. Its structure, featuring a benzophenone core and a spirocyclic moiety, makes it a valuable intermediate in the synthesis of compounds with biological activity. It is often employed in the creation of drug candidates targeting central nervous system disorders, as the trifluoromethyl group and the spirocyclic structure can enhance binding affinity and metabolic stability. Additionally, it serves as a key building block in the preparation of ligands for receptor studies, aiding in the exploration of biochemical pathways and drug discovery processes.
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