4-Chloro-2-(trifluoromethyl)nicotinic acid

≥95%

Reagent Code: #162212
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CAS Number 1018678-39-1

science Other reagents with same CAS 1018678-39-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.55 g/mol
Formula C₇H₃ClF₃NO₂
badge Registry Numbers
MDL Number MFCD22546902
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to enhance selectivity and biological activity. Its structure supports the development of compounds with improved environmental stability and target specificity. Also employed in the preparation of pharmaceuticals where the trifluoromethyl and chloro substituents contribute to metabolic resistance and binding affinity. Commonly utilized in research for designing new bioactive molecules in crop protection chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,200.00
inventory 1g
10-20 days ฿17,380.00
inventory 5g
10-20 days ฿65,530.00
inventory 250mg
10-20 days ฿5,470.00

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4-Chloro-2-(trifluoromethyl)nicotinic acid
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to enhance selectivity and biological activity. Its structure supports the development of compounds with improved environmental stability and target specificity. Also employed in the preparation of pharmaceuticals where the trifluoromethyl and chloro substituents contribute to metabolic resistance and binding affinity. Commonly utilized in research for designing new bioactive molecul

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to enhance selectivity and biological activity. Its structure supports the development of compounds with improved environmental stability and target specificity. Also employed in the preparation of pharmaceuticals where the trifluoromethyl and chloro substituents contribute to metabolic resistance and binding affinity. Commonly utilized in research for designing new bioactive molecules in crop protection chemistry.

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