ETHYL 4,6-DICHLORO-2-METHYLNICOTINATE

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Reagent Code: #182160
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CAS Number 686279-09-4

science Other reagents with same CAS 686279-09-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.081 g/mol
Formula C₉H₉Cl₂NO₂
badge Registry Numbers
MDL Number MFCD05666193
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of agrochemicals, particularly in the production of herbicides and plant growth regulators. Its chlorinated nicotinate structure makes it valuable for building active ingredients that target specific enzymes in weeds while minimizing impact on crops. Also utilized in research for developing new pesticide candidates due to its reactivity and ability to undergo substitution reactions. Commonly employed in the preparation of analogs for structure-activity relationship studies in crop protection chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿490.00
inventory 5g
10-20 days ฿2,200.00
inventory 25g
10-20 days ฿10,880.00
inventory 100g
10-20 days ฿40,050.00
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ETHYL 4,6-DICHLORO-2-METHYLNICOTINATE
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Used as an intermediate in the synthesis of agrochemicals, particularly in the production of herbicides and plant growth regulators. Its chlorinated nicotinate structure makes it valuable for building active ingredients that target specific enzymes in weeds while minimizing impact on crops. Also utilized in research for developing new pesticide candidates due to its reactivity and ability to undergo substitution reactions. Commonly employed in the preparation of analogs for structure-activity relationshi

Used as an intermediate in the synthesis of agrochemicals, particularly in the production of herbicides and plant growth regulators. Its chlorinated nicotinate structure makes it valuable for building active ingredients that target specific enzymes in weeds while minimizing impact on crops. Also utilized in research for developing new pesticide candidates due to its reactivity and ability to undergo substitution reactions. Commonly employed in the preparation of analogs for structure-activity relationship studies in crop protection chemistry.

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