Ethyl 1-amino-1H-imidazole-5-carboxylate

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Reagent Code: #183639
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CAS Number 1179361-84-2

science Other reagents with same CAS 1179361-84-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.16 g/mol
Formula C₆H₉N₃O₂
badge Registry Numbers
MDL Number MFCD12755702
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and antiviral agents. Its structure supports the formation of biologically active imidazole derivatives, which are common in drugs targeting enzyme systems in pathogens. Also employed in agrochemicals for the creation of plant protection compounds due to its reactivity and ability to form stable heterocyclic systems. Additionally, it serves in research settings for building blocks in medicinal chemistry and combinatorial library design.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,320.00
inventory 1g
10-20 days ฿5,240.00
inventory 5g
10-20 days ฿24,850.00
inventory 10g
10-20 days ฿45,170.00
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Ethyl 1-amino-1H-imidazole-5-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and antiviral agents. Its structure supports the formation of biologically active imidazole derivatives, which are common in drugs targeting enzyme systems in pathogens. Also employed in agrochemicals for the creation of plant protection compounds due to its reactivity and ability to form stable heterocyclic systems. Additionally, it serves in research settings for building blocks in medicinal ch

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and antiviral agents. Its structure supports the formation of biologically active imidazole derivatives, which are common in drugs targeting enzyme systems in pathogens. Also employed in agrochemicals for the creation of plant protection compounds due to its reactivity and ability to form stable heterocyclic systems. Additionally, it serves in research settings for building blocks in medicinal chemistry and combinatorial library design.

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