3,5-dichloro-2'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
97%
- Product Code: 75399
CAS:
898756-60-0
| Molecular Weight: | 406.31 g./mol | Molecular Formula: | C₂₁H₂₁Cl₂NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03842729 | |
| Melting Point: | Boiling Point: | 569.1℃ at 760 mmHg | |
| Density: | 1.36g/ml | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules. Its structure, featuring both a benzophenone core and a spirocyclic dioxa-aza moiety, makes it valuable for constructing pharmacologically active compounds. It is often employed in the development of drugs targeting neurological disorders, as the spirocyclic component can enhance binding affinity to specific receptors in the brain. Additionally, its dichloro-substituted benzophenone group is useful in UV-curable coatings and adhesives, where it acts as a photoinitiator to accelerate polymerization processes under UV light. The compound’s versatility also extends to materials science, where it is explored for creating advanced polymers with tailored properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €1,483.72 |
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| 2.000 | 10-20 days | €2,464.61 |
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3,5-dichloro-2'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules. Its structure, featuring both a benzophenone core and a spirocyclic dioxa-aza moiety, makes it valuable for constructing pharmacologically active compounds. It is often employed in the development of drugs targeting neurological disorders, as the spirocyclic component can enhance binding affinity to specific receptors in the brain. Additionally, its dichloro-substituted benzophenone group is useful in UV-curable coatings and adhesives, where it acts as a photoinitiator to accelerate polymerization processes under UV light. The compound’s versatility also extends to materials science, where it is explored for creating advanced polymers with tailored properties.
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