1-Benzyl-5-bromo-1H-imidazole
98%
- Product Code: 40277
CAS:
132430-59-2
| Molecular Weight: | 237.10 g./mol | Molecular Formula: | C₁₀H₉BrN₂ |
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| EC Number: | MDL Number: | MFCD19688638 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
1-Benzyl-5-bromo-1H-imidazole is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure, featuring both a benzyl group and a bromo substituent on the imidazole ring, makes it a versatile building block in medicinal chemistry. It is often employed in the synthesis of biologically active molecules, particularly in the creation of pharmaceuticals targeting various diseases. Additionally, it serves as a precursor in the preparation of ligands for metal-catalyzed reactions, aiding in the development of catalysts used in industrial processes. Its role in research extends to the study of heterocyclic chemistry, where it contributes to the exploration of new reaction pathways and the design of novel compounds with potential therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,605.00 |
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| 0.250 | 10-20 days | ฿15,210.00 |
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1-Benzyl-5-bromo-1H-imidazole
1-Benzyl-5-bromo-1H-imidazole is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure, featuring both a benzyl group and a bromo substituent on the imidazole ring, makes it a versatile building block in medicinal chemistry. It is often employed in the synthesis of biologically active molecules, particularly in the creation of pharmaceuticals targeting various diseases. Additionally, it serves as a precursor in the preparation of ligands for metal-catalyzed reactions, aiding in the development of catalysts used in industrial processes. Its role in research extends to the study of heterocyclic chemistry, where it contributes to the exploration of new reaction pathways and the design of novel compounds with potential therapeutic applications.
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