5-Phenyl-1H-imidazole-2-carbaldehyde

≥95%

Reagent Code: #226372
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CAS Number 56248-10-3

science Other reagents with same CAS 56248-10-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.18 g/mol
Formula C₁₀H₈N₂O
badge Registry Numbers
MDL Number MFCD10696709
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs with antifungal, antihypertensive, and anticancer activities. Its aldehyde functional group allows for easy modification and coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. Also employed in the preparation of ligands for metal-catalyzed reactions and in the fabrication of fluorescent probes due to its ability to form conjugated structures.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,400.00
inventory 250mg
10-20 days ฿3,440.00
inventory 1g
10-20 days ฿12,800.00
5-Phenyl-1H-imidazole-2-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs with antifungal, antihypertensive, and anticancer activities. Its aldehyde functional group allows for easy modification and coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. Also employed in the preparation of ligands for metal-catalyzed reactions and in the fabrication of fluorescent probes due to its ability to form conjugated stru
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs with antifungal, antihypertensive, and anticancer activities. Its aldehyde functional group allows for easy modification and coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. Also employed in the preparation of ligands for metal-catalyzed reactions and in the fabrication of fluorescent probes due to its ability to form conjugated structures.
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