N-(2-Bromo-6-fluorophenyl)-4,5-dihydro-1H-imidazol-2-amine hydrochloride
98%
- Product Code: 51649
CAS:
65896-14-2
Molecular Weight: | 294.5512 g./mol | Molecular Formula: | C₉H₁₀BrClFN₃ |
---|---|---|---|
EC Number: | MDL Number: | MFCD16293882 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. Its structure, featuring both a bromo and fluoro substituent on the aromatic ring, makes it a valuable intermediate in the creation of compounds targeting specific receptors or enzymes. It is often employed in the development of potential therapeutic agents, especially in areas such as central nervous system disorders, due to its ability to interact with various neurotransmitter systems. Additionally, its imidazole moiety contributes to its role in designing inhibitors or modulators for enzymes like kinases or proteases, which are critical in disease pathways. Its hydrochloride form enhances solubility, facilitating its use in experimental formulations and drug delivery systems.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
---|---|---|---|
0.100 | 10-20 days | £234.09 |
+
-
|
N-(2-Bromo-6-fluorophenyl)-4,5-dihydro-1H-imidazol-2-amine hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. Its structure, featuring both a bromo and fluoro substituent on the aromatic ring, makes it a valuable intermediate in the creation of compounds targeting specific receptors or enzymes. It is often employed in the development of potential therapeutic agents, especially in areas such as central nervous system disorders, due to its ability to interact with various neurotransmitter systems. Additionally, its imidazole moiety contributes to its role in designing inhibitors or modulators for enzymes like kinases or proteases, which are critical in disease pathways. Its hydrochloride form enhances solubility, facilitating its use in experimental formulations and drug delivery systems.
Mechanism | - |
Appearance | - |
Longevity | - |
Strength | - |
Storage | - |
Shelf Life | - |
Allergen(s) | - |
Dosage (Range) | - |
Recommended Dosage | - |
Dosage (Per Day) | - |
Recommended Dosage (Per Day) | - |
Mix Method | - |
Heat Resistance | - |
Stable in pH range | - |
Solubility | - |
Product Types | - |
INCI | - |
Cart
No products
Subtotal:
£0.00
£0.00
Total :