4,5-Diphenyl-1H-imidazole-2-carbaldehyde

≥95%

Reagent Code: #180301
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CAS Number 1465165-43-8

science Other reagents with same CAS 1465165-43-8

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scatter_plot Molecular Information
Weight 248.28 g/mol
Formula C₁₆H₁₂N₂O
badge Registry Numbers
MDL Number MFCD19058279
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, 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, anti-inflammatory, and anticancer properties. Its aldehyde functional group allows for easy modification, making it valuable in creating diverse derivatives for drug discovery. Also employed in the preparation of fluorescent dyes and sensors due to its ability to form conjugated systems that exhibit strong emission under UV light. Commonly used in organic synthesis for constructing nitrogen-containing heterocycles and in materials science for designing optoelectronic materials.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿39,600.00
inventory 250mg
10-20 days ฿17,500.00

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4,5-Diphenyl-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, anti-inflammatory, and anticancer properties. Its aldehyde functional group allows for easy modification, making it valuable in creating diverse derivatives for drug discovery. Also employed in the preparation of fluorescent dyes and sensors due to its ability to form conjugated systems that exhibit strong emission under UV light. Commonly used in organic synthesis for co
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs with antifungal, anti-inflammatory, and anticancer properties. Its aldehyde functional group allows for easy modification, making it valuable in creating diverse derivatives for drug discovery. Also employed in the preparation of fluorescent dyes and sensors due to its ability to form conjugated systems that exhibit strong emission under UV light. Commonly used in organic synthesis for constructing nitrogen-containing heterocycles and in materials science for designing optoelectronic materials.
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