2-chloro-6-(1H-imidazol-1-yl)benzenecarbonitrile

≥90%

Reagent Code: #197455
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CAS Number 287176-53-8

science Other reagents with same CAS 287176-53-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.63 g/mol
Formula C₁₀H₆ClN₃
badge Registry Numbers
MDL Number MFCD01764491
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in the synthesis of agricultural fungicides, particularly in the production of imidazole-based antifungal agents. Its structure enables effective inhibition of fungal growth in crop protection applications. It is especially valuable in systemic fungicides that target a broad spectrum of plant pathogens. Due to its nitrile and chloro-imidazole functional groups, it participates in coupling reactions and nucleophilic substitutions during the manufacturing of active pharmaceutical ingredients and agrochemicals. Its stability and reactivity profile make it suitable for use in both laboratory-scale and industrial-scale synthesis.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿7,380.00

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2-chloro-6-(1H-imidazol-1-yl)benzenecarbonitrile
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Used primarily as a key intermediate in the synthesis of agricultural fungicides, particularly in the production of imidazole-based antifungal agents. Its structure enables effective inhibition of fungal growth in crop protection applications. It is especially valuable in systemic fungicides that target a broad spectrum of plant pathogens. Due to its nitrile and chloro-imidazole functional groups, it participates in coupling reactions and nucleophilic substitutions during the manufacturing of active phar

Used primarily as a key intermediate in the synthesis of agricultural fungicides, particularly in the production of imidazole-based antifungal agents. Its structure enables effective inhibition of fungal growth in crop protection applications. It is especially valuable in systemic fungicides that target a broad spectrum of plant pathogens. Due to its nitrile and chloro-imidazole functional groups, it participates in coupling reactions and nucleophilic substitutions during the manufacturing of active pharmaceutical ingredients and agrochemicals. Its stability and reactivity profile make it suitable for use in both laboratory-scale and industrial-scale synthesis.

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