(1-Phenyl-1H-imidazol-4-yl)methanol
97%
- Product Code: 36148
CAS:
94128-94-6
| Molecular Weight: | 174.1992 g./mol | Molecular Formula: | C₁₀H₁₀N₂O |
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| EC Number: | MDL Number: | MFCD27933826 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
(1-Phenyl-1H-imidazol-4-yl)methanol is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly those targeting enzyme inhibition or receptor modulation. Its structure, featuring both an imidazole ring and a phenyl group, makes it a versatile building block for designing molecules with potential therapeutic applications, such as antifungal, antibacterial, or anti-inflammatory agents. Additionally, it is employed in the synthesis of ligands for metal coordination chemistry, which can be applied in catalysis or material science. The compound's hydroxyl group also allows for further functionalization, enabling the creation of more complex derivatives for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,754.00 |
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(1-Phenyl-1H-imidazol-4-yl)methanol
(1-Phenyl-1H-imidazol-4-yl)methanol is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly those targeting enzyme inhibition or receptor modulation. Its structure, featuring both an imidazole ring and a phenyl group, makes it a versatile building block for designing molecules with potential therapeutic applications, such as antifungal, antibacterial, or anti-inflammatory agents. Additionally, it is employed in the synthesis of ligands for metal coordination chemistry, which can be applied in catalysis or material science. The compound's hydroxyl group also allows for further functionalization, enabling the creation of more complex derivatives for drug discovery and development.
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