4-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
97%
- Product Code: 75590
CAS:
898757-37-4
Molecular Weight: | 337.42 g./mol | Molecular Formula: | C₂₁H₂₃NO₃ |
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EC Number: | MDL Number: | MFCD03841666 | |
Melting Point: | Boiling Point: | 483.6℃ at 760 mmHg | |
Density: | 1.22g/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 advanced materials and pharmaceuticals. Its structure, featuring a benzophenone moiety and a spirocyclic dioxa-aza system, makes it a valuable intermediate for creating complex molecules. It is often employed in photochemical applications due to the benzophenone group's ability to act as a photoinitiator or photosensitizer, enabling processes such as polymerization or crosslinking in UV-curable coatings and adhesives. Additionally, its unique spirocyclic component can be leveraged in the design of drug candidates, where it may contribute to enhanced stability, solubility, or bioavailability. Researchers also explore its potential in supramolecular chemistry for constructing novel molecular architectures with specific functional properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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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-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of advanced materials and pharmaceuticals. Its structure, featuring a benzophenone moiety and a spirocyclic dioxa-aza system, makes it a valuable intermediate for creating complex molecules. It is often employed in photochemical applications due to the benzophenone group's ability to act as a photoinitiator or photosensitizer, enabling processes such as polymerization or crosslinking in UV-curable coatings and adhesives. Additionally, its unique spirocyclic component can be leveraged in the design of drug candidates, where it may contribute to enhanced stability, solubility, or bioavailability. Researchers also explore its potential in supramolecular chemistry for constructing novel molecular architectures with specific functional properties.
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