Ethyl 5-fluoro-1H-imidazole-4-carboxylate
98%
- Product Code: 119861
CAS:
33235-31-3
Molecular Weight: | 158.130 g./mol | Molecular Formula: | C₆H₇FN₂O₂ |
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EC Number: | MDL Number: | MFCD21333183 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
Ethyl 5-fluoro-1H-imidazole-4-carboxylate is primarily utilized in the field of organic synthesis as a key intermediate for the development of various pharmaceutical compounds. Its structure, featuring both an imidazole ring and a carboxylate ester group, makes it a versatile building block in the synthesis of biologically active molecules. It is particularly valuable in the creation of antifungal and antibacterial agents, where the imidazole core is a critical component for activity. Additionally, this compound is employed in the research and development of new drugs targeting specific enzymes or receptors, leveraging its ability to interact with biological systems. Its fluoro substituent further enhances its potential in medicinal chemistry by influencing the pharmacokinetic properties of the resulting compounds.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿27,000.00 |
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Ethyl 5-fluoro-1H-imidazole-4-carboxylate
Ethyl 5-fluoro-1H-imidazole-4-carboxylate is primarily utilized in the field of organic synthesis as a key intermediate for the development of various pharmaceutical compounds. Its structure, featuring both an imidazole ring and a carboxylate ester group, makes it a versatile building block in the synthesis of biologically active molecules. It is particularly valuable in the creation of antifungal and antibacterial agents, where the imidazole core is a critical component for activity. Additionally, this compound is employed in the research and development of new drugs targeting specific enzymes or receptors, leveraging its ability to interact with biological systems. Its fluoro substituent further enhances its potential in medicinal chemistry by influencing the pharmacokinetic properties of the resulting compounds.
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