2-chloro-3'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]-4-fluorobenzophenone
97%
- Product Code: 75306
CAS:
898762-11-3
| Molecular Weight: | 389.86 g./mol | Molecular Formula: | C₂₁H₂₁ClFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03842212 | |
| Melting Point: | Boiling Point: | 516.8℃ at 760 mmHg | |
| Density: | 1.34g/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 pharmaceutical compounds. Its structure, featuring a benzophenone core with specific substitutions, makes it a valuable intermediate in the synthesis of complex molecules. The presence of the 1,4-dioxa-8-azaspiro[4.5]decyl group enhances its utility in creating compounds with potential biological activity, such as receptor ligands or enzyme inhibitors. Additionally, its chloro and fluoro substituents contribute to its reactivity and selectivity in various chemical reactions, making it a key component in the design of new drugs or bioactive molecules. Its application is often seen in research settings where precise molecular modifications are required to achieve desired pharmacological properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿56,240.00 |
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| 2.000 | 10-20 days | ฿93,420.00 |
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2-chloro-3'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]-4-fluorobenzophenone
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. Its structure, featuring a benzophenone core with specific substitutions, makes it a valuable intermediate in the synthesis of complex molecules. The presence of the 1,4-dioxa-8-azaspiro[4.5]decyl group enhances its utility in creating compounds with potential biological activity, such as receptor ligands or enzyme inhibitors. Additionally, its chloro and fluoro substituents contribute to its reactivity and selectivity in various chemical reactions, making it a key component in the design of new drugs or bioactive molecules. Its application is often seen in research settings where precise molecular modifications are required to achieve desired pharmacological properties.
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