6-(Chloromethyl)-11H-dibenzo[b,e]azepine
95%
- Product Code: 87631
CAS:
21535-44-4
| Molecular Weight: | 241.72 g./mol | Molecular Formula: | C₁₅H₁₂ClN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02167647 | |
| Melting Point: | Boiling Point: | 351 °C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, store under inert gas |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring a chloromethyl group attached to a dibenzoazepine core, makes it a valuable building block for creating molecules with potential therapeutic properties. Researchers often employ it in the development of drugs targeting neurological disorders, such as anxiety, depression, and epilepsy, due to its ability to interact with specific receptors in the brain. Additionally, it is used in the synthesis of compounds with potential anti-inflammatory and analgesic effects. Its versatility in chemical reactions, such as nucleophilic substitution, allows for the creation of diverse derivatives, further expanding its applications in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,338.00 |
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| 0.250 | 10-20 days | ฿6,498.00 |
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| 1.000 | 10-20 days | ฿16,254.00 |
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6-(Chloromethyl)-11H-dibenzo[b,e]azepine
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring a chloromethyl group attached to a dibenzoazepine core, makes it a valuable building block for creating molecules with potential therapeutic properties. Researchers often employ it in the development of drugs targeting neurological disorders, such as anxiety, depression, and epilepsy, due to its ability to interact with specific receptors in the brain. Additionally, it is used in the synthesis of compounds with potential anti-inflammatory and analgesic effects. Its versatility in chemical reactions, such as nucleophilic substitution, allows for the creation of diverse derivatives, further expanding its applications in medicinal chemistry.
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