1,2,3,4,5,6-Hexahydrobenzo[b]azocine
97%
- Product Code: 38771
CAS:
7124-93-8
| Molecular Weight: | 161.2435 g./mol | Molecular Formula: | C₁₁H₁₅N |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12755898 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its unique structure, featuring an azocine ring fused to a cyclohexane moiety, makes it a valuable scaffold for developing compounds with potential therapeutic effects. Researchers have explored its use in creating analogs that target central nervous system disorders, such as anxiety, depression, and pain management, due to its ability to interact with neurotransmitter receptors. Additionally, it has been investigated for its potential in designing drugs with anti-inflammatory and analgesic properties. Its versatility in chemical modifications allows for the development of novel compounds with optimized biological activity and reduced side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,795.00 |
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1,2,3,4,5,6-Hexahydrobenzo[b]azocine
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its unique structure, featuring an azocine ring fused to a cyclohexane moiety, makes it a valuable scaffold for developing compounds with potential therapeutic effects. Researchers have explored its use in creating analogs that target central nervous system disorders, such as anxiety, depression, and pain management, due to its ability to interact with neurotransmitter receptors. Additionally, it has been investigated for its potential in designing drugs with anti-inflammatory and analgesic properties. Its versatility in chemical modifications allows for the development of novel compounds with optimized biological activity and reduced side effects.
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