Ethyl 1H-imidazole-1-carboxylate

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Reagent Code: #183486
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CAS Number 19213-72-0

science Other reagents with same CAS 19213-72-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 140.14 g/mol
Formula C₆H₈N₂O₂
badge Registry Numbers
MDL Number MFCD00014498
thermostat Physical Properties
Boiling Point 71-72°C
inventory_2 Storage & Handling
Density 1.27g/cm3
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protecting group for imidazole derivatives during peptide synthesis and other multi-step reactions. Its reactivity allows for efficient introduction of the imidazole ring into larger molecules, making it valuable in drug development, especially in histidine-related compounds and kinase inhibitors. Also employed in the synthesis of ionic liquids and functional materials due to its stable ester and heterocyclic structure.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿310.00
inventory 5g
10-20 days ฿1,300.00
inventory 10g
10-20 days ฿2,410.00
inventory 25g
10-20 days ฿6,010.00

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Ethyl 1H-imidazole-1-carboxylate
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protecting group for imidazole derivatives during peptide synthesis and other multi-step reactions. Its reactivity allows for efficient introduction of the imidazole ring into larger molecules, making it valuable in drug development, especially in histidine-related compounds and kinase inhibitors. Also employed in the synthesis of ionic liquids and functional materials due

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protecting group for imidazole derivatives during peptide synthesis and other multi-step reactions. Its reactivity allows for efficient introduction of the imidazole ring into larger molecules, making it valuable in drug development, especially in histidine-related compounds and kinase inhibitors. Also employed in the synthesis of ionic liquids and functional materials due to its stable ester and heterocyclic structure.

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