Methyl 6-chloro-5-(trifluoromethyl)picolinate

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Reagent Code: #209050
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CAS Number 1211518-35-2

science Other reagents with same CAS 1211518-35-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.58 g/mol
Formula C₈H₅ClF₃NO₂
badge Registry Numbers
MDL Number MFCD18255501
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of agricultural chemicals, particularly in the production of herbicides and insecticides. Its structure allows for further functionalization to create active ingredients that target specific pests or weeds. Commonly employed in the development of fluorine-containing agrochemicals due to enhanced bioavailability and stability imparted by the trifluoromethyl group. Also utilized in research for novel crop protection agents owing to its reactivity in coupling and substitution reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,120.00
inventory 250mg
10-20 days ฿2,780.00
inventory 1g
10-20 days ฿7,970.00

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Methyl 6-chloro-5-(trifluoromethyl)picolinate
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Used as a key intermediate in the synthesis of agricultural chemicals, particularly in the production of herbicides and insecticides. Its structure allows for further functionalization to create active ingredients that target specific pests or weeds. Commonly employed in the development of fluorine-containing agrochemicals due to enhanced bioavailability and stability imparted by the trifluoromethyl group. Also utilized in research for novel crop protection agents owing to its reactivity in coupling and sub
Used as a key intermediate in the synthesis of agricultural chemicals, particularly in the production of herbicides and insecticides. Its structure allows for further functionalization to create active ingredients that target specific pests or weeds. Commonly employed in the development of fluorine-containing agrochemicals due to enhanced bioavailability and stability imparted by the trifluoromethyl group. Also utilized in research for novel crop protection agents owing to its reactivity in coupling and substitution reactions.
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