Ethyl 4-chloro-6-(trifluoromethyl)nicotinate

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Reagent Code: #182755
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CAS Number 1196146-35-6

science Other reagents with same CAS 1196146-35-6

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Weight 253.61 g/mol
Formula C₉H₇ClF₃NO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and insecticides. Its structure allows for the introduction of fluorinated moieties, enhancing the bioavailability and metabolic stability of active ingredients. Commonly employed in the production of nicotinic receptor-targeting pesticides, it contributes to improved pest control efficacy with lower application rates. Also utilized in medicinal chemistry research for designing novel bioactive molecules due to its electron-withdrawing groups and aromatic functionality.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,790.00
inventory 500mg
10-20 days ฿7,000.00
inventory 1g
10-20 days ฿12,000.00

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Ethyl 4-chloro-6-(trifluoromethyl)nicotinate
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Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and insecticides. Its structure allows for the introduction of fluorinated moieties, enhancing the bioavailability and metabolic stability of active ingredients. Commonly employed in the production of nicotinic receptor-targeting pesticides, it contributes to improved pest control efficacy with lower application rates. Also utilized in medicinal chemistry research for designing novel bioactive molecul
Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and insecticides. Its structure allows for the introduction of fluorinated moieties, enhancing the bioavailability and metabolic stability of active ingredients. Commonly employed in the production of nicotinic receptor-targeting pesticides, it contributes to improved pest control efficacy with lower application rates. Also utilized in medicinal chemistry research for designing novel bioactive molecules due to its electron-withdrawing groups and aromatic functionality.
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