1-(4-Bromo-2-fluorophenyl)ethanamine hydrochloride
95%
- Product Code: 73230
CAS:
1909319-65-8
| Molecular Weight: | 254.53 g./mol | Molecular Formula: | C₈H₁₀BrClFN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29763070 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring both bromo and fluoro substituents, makes it valuable for designing compounds with potential therapeutic applications, particularly in the development of central nervous system (CNS) drugs. Researchers often employ it to explore its interactions with biological targets, such as receptors or enzymes, to develop new treatments for neurological disorders. Additionally, its halogenated aromatic ring system is useful in medicinal chemistry for optimizing drug potency and selectivity. The hydrochloride salt form enhances its stability and solubility, facilitating its use in experimental and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,529.00 |
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| 0.250 | 10-20 days | ฿4,554.00 |
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| 1.000 | 10-20 days | ฿14,040.00 |
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1-(4-Bromo-2-fluorophenyl)ethanamine hydrochloride
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring both bromo and fluoro substituents, makes it valuable for designing compounds with potential therapeutic applications, particularly in the development of central nervous system (CNS) drugs. Researchers often employ it to explore its interactions with biological targets, such as receptors or enzymes, to develop new treatments for neurological disorders. Additionally, its halogenated aromatic ring system is useful in medicinal chemistry for optimizing drug potency and selectivity. The hydrochloride salt form enhances its stability and solubility, facilitating its use in experimental and industrial processes.
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