3-Chloro-4-(trifluoromethoxy)benzonitrile

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Reagent Code: #159674
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CAS Number 129604-26-8

science Other reagents with same CAS 129604-26-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.57 g/mol
Formula C₈H₃ClF₃NO
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MDL Number MFCD01631557
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of agricultural chemicals, particularly herbicides and insecticides. Its structure supports the development of active ingredients that target specific enzymes in pests or unwanted plants, improving selectivity and efficacy. The nitrile and trifluoromethoxy groups enhance lipophilicity and metabolic stability, making it valuable in designing compounds with improved environmental persistence and uptake. Also employed in the preparation of pharmaceuticals where aromatic nitriles serve as precursors to heterocyclic systems. Commonly utilized in research and development for new crop protection agents due to its reactivity and functional group compatibility.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,310.00
inventory 25g
10-20 days ฿10,880.00
inventory 100g
10-20 days ฿43,510.00

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3-Chloro-4-(trifluoromethoxy)benzonitrile
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Used as a key intermediate in the synthesis of agricultural chemicals, particularly herbicides and insecticides. Its structure supports the development of active ingredients that target specific enzymes in pests or unwanted plants, improving selectivity and efficacy. The nitrile and trifluoromethoxy groups enhance lipophilicity and metabolic stability, making it valuable in designing compounds with improved environmental persistence and uptake. Also employed in the preparation of pharmaceuticals where ar

Used as a key intermediate in the synthesis of agricultural chemicals, particularly herbicides and insecticides. Its structure supports the development of active ingredients that target specific enzymes in pests or unwanted plants, improving selectivity and efficacy. The nitrile and trifluoromethoxy groups enhance lipophilicity and metabolic stability, making it valuable in designing compounds with improved environmental persistence and uptake. Also employed in the preparation of pharmaceuticals where aromatic nitriles serve as precursors to heterocyclic systems. Commonly utilized in research and development for new crop protection agents due to its reactivity and functional group compatibility.

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