4-bromo-4'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
97%
- Product Code: 75615
CAS:
898757-78-3
| Molecular Weight: | 416.32 g./mol | Molecular Formula: | C₂₁H₂₂BrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03841682 | |
| Melting Point: | Boiling Point: | 522.7℃ at 760 mmHg | |
| Density: | 1.44g/ml | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of advanced materials and pharmaceuticals. Its structure, featuring a benzophenone core and a dioxa-azaspiro moiety, makes it a valuable intermediate for constructing complex molecules. It is often employed in the synthesis of photoresponsive materials due to its ability to undergo light-induced reactions, which is useful in creating light-sensitive polymers or coatings. Additionally, its spirocyclic component is leveraged in medicinal chemistry for designing drug candidates with enhanced stability and bioavailability. The bromine atom further allows for functionalization through cross-coupling reactions, enabling the creation of diverse chemical architectures for research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $1,687.37 |
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| 2.000 | 10-20 days | $2,802.88 |
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4-bromo-4'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
This compound is primarily utilized in the field of organic synthesis, particularly in the development of advanced materials and pharmaceuticals. Its structure, featuring a benzophenone core and a dioxa-azaspiro moiety, makes it a valuable intermediate for constructing complex molecules. It is often employed in the synthesis of photoresponsive materials due to its ability to undergo light-induced reactions, which is useful in creating light-sensitive polymers or coatings. Additionally, its spirocyclic component is leveraged in medicinal chemistry for designing drug candidates with enhanced stability and bioavailability. The bromine atom further allows for functionalization through cross-coupling reactions, enabling the creation of diverse chemical architectures for research and industrial applications.
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