Diethyl 1H-imidazole-4,5-dicarboxylate

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Reagent Code: #177818
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CAS Number 1080-79-1

science Other reagents with same CAS 1080-79-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.20 g/mol
Formula C₉H₁₂N₂O₄
badge Registry Numbers
MDL Number MFCD00723829
thermostat Physical Properties
Melting Point 153-157 °C
Boiling Point 357.9 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs which exhibit antifungal, antihypertensive, and anticancer activities. It serves as a building block in medicinal chemistry due to the reactivity of its ester groups and the presence of the imidazole ring, which is common in bioactive molecules. It is also employed in the preparation of ligands for catalysis and in the fabrication of functional materials where nitrogen-containing heterocycles are required. Its solubility and stability make it suitable for use in various organic transformations, including cross-coupling and condensation reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,920.00
inventory 5g
10-20 days ฿7,140.00

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Diethyl 1H-imidazole-4,5-dicarboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs which exhibit antifungal, antihypertensive, and anticancer activities. It serves as a building block in medicinal chemistry due to the reactivity of its ester groups and the presence of the imidazole ring, which is common in bioactive molecules. It is also employed in the preparation of ligands for catalysis and in the fabrication of functional materials where nitrogen-containing heter

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs which exhibit antifungal, antihypertensive, and anticancer activities. It serves as a building block in medicinal chemistry due to the reactivity of its ester groups and the presence of the imidazole ring, which is common in bioactive molecules. It is also employed in the preparation of ligands for catalysis and in the fabrication of functional materials where nitrogen-containing heterocycles are required. Its solubility and stability make it suitable for use in various organic transformations, including cross-coupling and condensation reactions.

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