1-Ethyl-1H-imidazole-2-carbaldehyde

≥95%

Reagent Code: #182373
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CAS Number 111851-98-0

science Other reagents with same CAS 111851-98-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 124.14 g/mol
Formula C₆H₈N₂O
thermostat Physical Properties
Boiling Point 258°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure supports the formation of biologically active imidazole derivatives. Also employed in agrochemicals for creating fungicides and plant growth regulators. Serves as a building block in coordination chemistry for preparing metal-organic frameworks and catalysts. Its aldehyde group allows for easy functionalization, enabling use in Schiff base formation and multistep organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿320.00
inventory 5g
10-20 days ฿750.00
inventory 250mg
10-20 days ฿180.00
inventory 25g
10-20 days ฿3,420.00
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1-Ethyl-1H-imidazole-2-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure supports the formation of biologically active imidazole derivatives. Also employed in agrochemicals for creating fungicides and plant growth regulators. Serves as a building block in coordination chemistry for preparing metal-organic frameworks and catalysts. Its aldehyde group allows for easy functionalization, enabling use in Schiff base formation and multistep
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure supports the formation of biologically active imidazole derivatives. Also employed in agrochemicals for creating fungicides and plant growth regulators. Serves as a building block in coordination chemistry for preparing metal-organic frameworks and catalysts. Its aldehyde group allows for easy functionalization, enabling use in Schiff base formation and multistep organic synthesis.
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