2-Bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-4-carbonitrile
95%
- Product Code: 43107
CAS:
854044-51-2
| Molecular Weight: | 302.2430 g./mol | Molecular Formula: | C₁₀H₁₆BrN₃OSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12964153 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of complex molecules, particularly in pharmaceutical research. Its structure, featuring a bromo group and a protected imidazole ring, makes it valuable for constructing biologically active compounds, such as inhibitors or ligands targeting specific enzymes or receptors. The trimethylsilyl-protected group enhances stability during synthetic processes, allowing for selective deprotection and further functionalization. It is often employed in the development of drug candidates, especially in the fields of oncology and infectious diseases, where imidazole derivatives play a critical role. Additionally, its carbonitrile moiety offers opportunities for further chemical modifications, enabling the creation of diverse molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $199.62 |
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2-Bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-4-carbonitrile
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of complex molecules, particularly in pharmaceutical research. Its structure, featuring a bromo group and a protected imidazole ring, makes it valuable for constructing biologically active compounds, such as inhibitors or ligands targeting specific enzymes or receptors. The trimethylsilyl-protected group enhances stability during synthetic processes, allowing for selective deprotection and further functionalization. It is often employed in the development of drug candidates, especially in the fields of oncology and infectious diseases, where imidazole derivatives play a critical role. Additionally, its carbonitrile moiety offers opportunities for further chemical modifications, enabling the creation of diverse molecular architectures.
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