4-(1H-1,2,4-Triazolylmethyl)benzonitrile

90%

Reagent Code: #196676
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CAS Number 112809-25-3

science Other reagents with same CAS 112809-25-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.1973 g/mol
Formula C₁₀H₈N₄
badge Registry Numbers
MDL Number MFCD07368016
thermostat Physical Properties
Melting Point 69-72℃
Boiling Point 412.1℃ at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of antifungal agents, particularly in the production of triazole-based pharmaceuticals like fluconazole and related derivatives. Its nitrile and triazole functionalities allow for further chemical modifications, making it valuable in medicinal chemistry for developing bioactive molecules. It is also employed in the preparation of agrochemicals and functional materials due to its ability to form stable complexes and participate in click chemistry reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,680.00

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4-(1H-1,2,4-Triazolylmethyl)benzonitrile
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Used as a key intermediate in the synthesis of antifungal agents, particularly in the production of triazole-based pharmaceuticals like fluconazole and related derivatives. Its nitrile and triazole functionalities allow for further chemical modifications, making it valuable in medicinal chemistry for developing bioactive molecules. It is also employed in the preparation of agrochemicals and functional materials due to its ability to form stable complexes and participate in click chemistry reactions.
Used as a key intermediate in the synthesis of antifungal agents, particularly in the production of triazole-based pharmaceuticals like fluconazole and related derivatives. Its nitrile and triazole functionalities allow for further chemical modifications, making it valuable in medicinal chemistry for developing bioactive molecules. It is also employed in the preparation of agrochemicals and functional materials due to its ability to form stable complexes and participate in click chemistry reactions.
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