4-(4H-1,2,4-Triazol-3-yl)aniline

96%

Reagent Code: #195576
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CAS Number 4922-51-4

science Other reagents with same CAS 4922-51-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.18 g/mol
Formula C₈H₈N₄
badge Registry Numbers
MDL Number MFCD07643239
thermostat Physical Properties
Boiling Point 418.6±47.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antifungal agents like fluconazole and voriconazole. It plays a crucial role in constructing triazole-based drug molecules due to its ability to link aromatic and heterocyclic systems. Also employed in the development of agrochemicals and functional materials where nitrogen-rich heterocycles enhance biological activity or material stability. Its amine group allows for easy derivatization, making it valuable in medicinal chemistry for building diverse compound libraries.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,750.00

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4-(4H-1,2,4-Triazol-3-yl)aniline
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antifungal agents like fluconazole and voriconazole. It plays a crucial role in constructing triazole-based drug molecules due to its ability to link aromatic and heterocyclic systems. Also employed in the development of agrochemicals and functional materials where nitrogen-rich heterocycles enhance biological activity or material stability. Its amine group allows for easy derivatization, making it valuable in medicinal chemi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antifungal agents like fluconazole and voriconazole. It plays a crucial role in constructing triazole-based drug molecules due to its ability to link aromatic and heterocyclic systems. Also employed in the development of agrochemicals and functional materials where nitrogen-rich heterocycles enhance biological activity or material stability. Its amine group allows for easy derivatization, making it valuable in medicinal chemistry for building diverse compound libraries.

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