2-chloro-4'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
97%
- Product Code: 75310
CAS:
898758-06-0
| Molecular Weight: | 371.87 g./mol | Molecular Formula: | C₂₁H₂₂ClNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03841695 | |
| Melting Point: | Boiling Point: | 510.4℃ at 760 mmHg | |
| Density: | 1.29g/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 pharmaceuticals and bioactive compounds. Its structure, featuring a benzophenone core and a dioxa-azaspiro moiety, makes it a valuable intermediate for constructing complex molecules. It is often employed in the synthesis of compounds with potential therapeutic applications, such as central nervous system (CNS) agents or enzyme inhibitors. Additionally, its unique spirocyclic structure can be leveraged in materials science for designing novel polymers or functional materials with specific optical or electronic properties. Researchers also explore its use in photochemistry due to the benzophenone group, which can act as a photosensitizer in various reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿58,110.00 |
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| 2.000 | 10-20 days | ฿96,540.00 |
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2-chloro-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 pharmaceuticals and bioactive compounds. Its structure, featuring a benzophenone core and a dioxa-azaspiro moiety, makes it a valuable intermediate for constructing complex molecules. It is often employed in the synthesis of compounds with potential therapeutic applications, such as central nervous system (CNS) agents or enzyme inhibitors. Additionally, its unique spirocyclic structure can be leveraged in materials science for designing novel polymers or functional materials with specific optical or electronic properties. Researchers also explore its use in photochemistry due to the benzophenone group, which can act as a photosensitizer in various reactions.
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