4'-carboethoxy-2-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
97%
- Product Code: 75535
CAS:
898755-92-5
| Molecular Weight: | 409.49 g./mol | Molecular Formula: | C₂₄H₂₇NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03842699 | |
| Melting Point: | Boiling Point: | 577℃ at 760 mmHg | |
| Density: | 1.25g/ml | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active molecules, including potential drug candidates. Its structure, featuring a benzophenone core and functional groups like carboethoxy and dioxa-azaspiro, makes it valuable for designing compounds with specific binding properties. It is often employed in medicinal chemistry to create molecules that target enzymes or receptors, aiding in the discovery of new therapeutic agents. Additionally, its spirocyclic moiety contributes to the stability and conformational rigidity of the synthesized compounds, enhancing their efficacy in biological systems.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿56,240.00 |
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| 2.000 | 10-20 days | ฿93,420.00 |
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4'-carboethoxy-2-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active molecules, including potential drug candidates. Its structure, featuring a benzophenone core and functional groups like carboethoxy and dioxa-azaspiro, makes it valuable for designing compounds with specific binding properties. It is often employed in medicinal chemistry to create molecules that target enzymes or receptors, aiding in the discovery of new therapeutic agents. Additionally, its spirocyclic moiety contributes to the stability and conformational rigidity of the synthesized compounds, enhancing their efficacy in biological systems.
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