2-(1H-Imidazol-1-yl)ethanamine dihydrochloride
98%
- Product Code: 71900
CAS:
93668-43-0
| Molecular Weight: | 184.07 g./mol | Molecular Formula: | C₅H₁₁Cl₂N₃ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 214-216°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in biochemical research and pharmaceutical development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition or receptor modulation. Its imidazole moiety makes it valuable in designing compounds for antifungal, antibacterial, and anti-inflammatory applications. Additionally, it is employed in the preparation of ligands for metal coordination studies, aiding in the development of catalysts or materials with specific properties. Its role in medicinal chemistry is significant, often contributing to the creation of novel therapeutic agents.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to yellow to brown powder or crystals |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €62.00 |
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| 1.000 | 10-20 days | €163.04 |
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2-(1H-Imidazol-1-yl)ethanamine dihydrochloride
This compound is primarily utilized in biochemical research and pharmaceutical development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition or receptor modulation. Its imidazole moiety makes it valuable in designing compounds for antifungal, antibacterial, and anti-inflammatory applications. Additionally, it is employed in the preparation of ligands for metal coordination studies, aiding in the development of catalysts or materials with specific properties. Its role in medicinal chemistry is significant, often contributing to the creation of novel therapeutic agents.
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