1-(4-Bromophenyl)cyclobutanamine hydrochloride
97%
- Product Code: 71738
CAS:
1193389-40-0
| Molecular Weight: | 262.57 g./mol | Molecular Formula: | C₁₀H₁₃BrClN |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a cyclobutane ring and a bromophenyl group, makes it a valuable intermediate in the creation of molecules targeting central nervous system disorders. Researchers utilize it to explore potential treatments for conditions like depression, anxiety, and chronic pain due to its ability to interact with specific neurotransmitter systems. Additionally, it serves as a building block in organic chemistry for constructing more complex molecules with potential therapeutic applications. Its hydrochloride form ensures stability and solubility, facilitating its use in various experimental protocols.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | $45.66 |
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| 0.100 | 10-20 days | $127.42 |
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1-(4-Bromophenyl)cyclobutanamine hydrochloride
This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a cyclobutane ring and a bromophenyl group, makes it a valuable intermediate in the creation of molecules targeting central nervous system disorders. Researchers utilize it to explore potential treatments for conditions like depression, anxiety, and chronic pain due to its ability to interact with specific neurotransmitter systems. Additionally, it serves as a building block in organic chemistry for constructing more complex molecules with potential therapeutic applications. Its hydrochloride form ensures stability and solubility, facilitating its use in various experimental protocols.
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