2,3-dimethyl-3'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
97%
- Product Code: 75059
CAS:
898761-81-4
| Molecular Weight: | 365.48 g./mol | Molecular Formula: | C₂₃H₂₇NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03842198 | |
| Melting Point: | Boiling Point: | 507.9℃ at 760 mmHg | |
| Density: | 1.19g/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 photoresponsive materials. Its structure, which includes a benzophenone moiety, makes it suitable for applications in photochemistry, where it can act as a photoinitiator or photosensitizer. The presence of the 1,4-dioxa-8-azaspiro[4.5]decyl group enhances its solubility and stability, making it effective in polymer chemistry for creating cross-linked networks under UV light exposure. Additionally, it finds use in the production of advanced coatings, adhesives, and inks that require light-induced curing processes. Its unique molecular design also allows for potential applications in biomedical research, particularly in the development of light-activated drug delivery systems or photodynamic therapy agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft605,935.83 |
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| 2.000 | 10-20 days | Ft1,006,517.17 |
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2,3-dimethyl-3'-[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 photoresponsive materials. Its structure, which includes a benzophenone moiety, makes it suitable for applications in photochemistry, where it can act as a photoinitiator or photosensitizer. The presence of the 1,4-dioxa-8-azaspiro[4.5]decyl group enhances its solubility and stability, making it effective in polymer chemistry for creating cross-linked networks under UV light exposure. Additionally, it finds use in the production of advanced coatings, adhesives, and inks that require light-induced curing processes. Its unique molecular design also allows for potential applications in biomedical research, particularly in the development of light-activated drug delivery systems or photodynamic therapy agents.
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