3,5-dimethyl-4'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
97%
- Product Code: 75407
CAS:
898757-98-7
| Molecular Weight: | 365.48 g./mol | Molecular Formula: | C₂₃H₂₇NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03841692 | |
| Melting Point: | Boiling Point: | 527.9℃ at 760 mmHg | |
| Density: | 1.19g/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 unique structure makes it valuable as a building block for creating complex molecules, especially those requiring specific photochemical properties. It is often employed in the synthesis of light-sensitive compounds used in photoresists for semiconductor manufacturing. Additionally, its benzophenone moiety is useful in UV-curable coatings and adhesives, where it acts as a photoinitiator to trigger polymerization under UV light. The compound’s spirocyclic component also lends itself to applications in drug discovery, where it can be incorporated into molecules to enhance their stability and bioavailability. Its versatility makes it a key intermediate in research and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | £1,271.98 |
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| 2.000 | 10-20 days | £2,112.88 |
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3,5-dimethyl-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 unique structure makes it valuable as a building block for creating complex molecules, especially those requiring specific photochemical properties. It is often employed in the synthesis of light-sensitive compounds used in photoresists for semiconductor manufacturing. Additionally, its benzophenone moiety is useful in UV-curable coatings and adhesives, where it acts as a photoinitiator to trigger polymerization under UV light. The compound’s spirocyclic component also lends itself to applications in drug discovery, where it can be incorporated into molecules to enhance their stability and bioavailability. Its versatility makes it a key intermediate in research and industrial processes.
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