1-(3-Bromopropyl)-1H-imidazole hydrobromide
95%
- Product Code: 123786
CAS:
109914-45-6
| Molecular Weight: | 269.965 g./mol | Molecular Formula: | C₆H₁₀Br₂N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18917307 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dark, inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. It is often employed in the development of pharmaceutical compounds, particularly in the synthesis of imidazole derivatives, which are known for their biological activity. The compound serves as a key intermediate in the creation of potential drug candidates targeting various therapeutic areas, including antifungal, antibacterial, and anticancer agents. Additionally, it is used in research settings to study the reactivity and functionalization of imidazole rings, which are important structures in medicinal chemistry. Its bromopropyl group allows for further modifications, making it valuable in the design and synthesis of novel chemical entities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,656.00 |
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| 0.250 | 10-20 days | ฿2,808.00 |
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| 1.000 | 10-20 days | ฿7,578.00 |
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1-(3-Bromopropyl)-1H-imidazole hydrobromide
This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. It is often employed in the development of pharmaceutical compounds, particularly in the synthesis of imidazole derivatives, which are known for their biological activity. The compound serves as a key intermediate in the creation of potential drug candidates targeting various therapeutic areas, including antifungal, antibacterial, and anticancer agents. Additionally, it is used in research settings to study the reactivity and functionalization of imidazole rings, which are important structures in medicinal chemistry. Its bromopropyl group allows for further modifications, making it valuable in the design and synthesis of novel chemical entities.
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