Ethyl 2-(1H-imidazol-4-yl)acetate

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Reagent Code: #41247
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CAS Number 28782-45-8

science Other reagents with same CAS 28782-45-8

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Weight 154.1665 g/mol
Formula C₇H₁₀N₂O₂
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Ethyl 2-(1H-imidazol-4-yl)acetate is primarily used in organic synthesis as a key intermediate in the production of various pharmaceutical compounds. It plays a significant role in the development of histamine-related drugs, particularly those targeting histamine receptors, which are crucial in treating allergies, gastric acid secretion disorders, and other medical conditions. Additionally, this compound is utilized in the synthesis of biologically active molecules, including antifungal and antibacterial agents, due to the imidazole ring's ability to interact with enzymes and proteins. Its ester group also makes it a versatile building block for further chemical modifications in drug discovery and development processes.

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inventory 100mg
10-20 days ฿2,826.00

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Ethyl 2-(1H-imidazol-4-yl)acetate
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Ethyl 2-(1H-imidazol-4-yl)acetate is primarily used in organic synthesis as a key intermediate in the production of various pharmaceutical compounds. It plays a significant role in the development of histamine-related drugs, particularly those targeting histamine receptors, which are crucial in treating allergies, gastric acid secretion disorders, and other medical conditions. Additionally, this compound is utilized in the synthesis of biologically active molecules, including antifungal and antibacterial

Ethyl 2-(1H-imidazol-4-yl)acetate is primarily used in organic synthesis as a key intermediate in the production of various pharmaceutical compounds. It plays a significant role in the development of histamine-related drugs, particularly those targeting histamine receptors, which are crucial in treating allergies, gastric acid secretion disorders, and other medical conditions. Additionally, this compound is utilized in the synthesis of biologically active molecules, including antifungal and antibacterial agents, due to the imidazole ring's ability to interact with enzymes and proteins. Its ester group also makes it a versatile building block for further chemical modifications in drug discovery and development processes.

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