4'-chloro-3-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benozphenone
97%
- Product Code: 75531
CAS:
898761-75-6
| Molecular Weight: | 371.87 g./mol | Molecular Formula: | C₂₁H₂₂ClNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03842195 | |
| Melting Point: | Boiling Point: | 517.5℃ at 760 mmHg | |
| Density: | 1.29g/ml | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the development of more complex chemical structures. Its unique structure, featuring a chloro-substituted benzophenone and a dioxa-azaspiro moiety, makes it valuable for constructing molecules with specific pharmacological properties. Researchers often employ it in the synthesis of potential drug candidates, especially those targeting neurological or psychiatric disorders, due to its ability to interact with biological systems. Additionally, it may be used in material science for creating advanced polymers or coatings with tailored properties, leveraging its reactive functional groups for cross-linking or modification purposes.
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'-chloro-3-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benozphenone
This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the development of more complex chemical structures. Its unique structure, featuring a chloro-substituted benzophenone and a dioxa-azaspiro moiety, makes it valuable for constructing molecules with specific pharmacological properties. Researchers often employ it in the synthesis of potential drug candidates, especially those targeting neurological or psychiatric disorders, due to its ability to interact with biological systems. Additionally, it may be used in material science for creating advanced polymers or coatings with tailored properties, leveraging its reactive functional groups for cross-linking or modification purposes.
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