3-Chlor-2-(2-Chlor-5-Amino-Phenoxy)-5-(Trifluoromethyl)-Pyridine

≥97%

Reagent Code: #69910
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CAS Number 87170-48-7

science Other reagents with same CAS 87170-48-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.1 g/mol
Formula C₁₂H₇Cl₂F₃N₂O
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in the agricultural sector as a key intermediate in the synthesis of advanced herbicides. Its structure allows it to act as a building block for creating compounds that effectively target and control the growth of unwanted weeds in crops. The presence of the trifluoromethyl group enhances the herbicidal activity, making it particularly effective against a broad spectrum of weed species. Additionally, its chemical properties contribute to the development of formulations that are stable and efficient under various environmental conditions, ensuring prolonged efficacy in the field. Researchers also explore its potential in developing new agrochemicals with improved safety profiles and reduced environmental impact.

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Test Parameter Specification
Appearance Brown Solid
Purity (%) 97-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿4,725.00

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3-Chlor-2-(2-Chlor-5-Amino-Phenoxy)-5-(Trifluoromethyl)-Pyridine
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This chemical is primarily utilized in the agricultural sector as a key intermediate in the synthesis of advanced herbicides. Its structure allows it to act as a building block for creating compounds that effectively target and control the growth of unwanted weeds in crops. The presence of the trifluoromethyl group enhances the herbicidal activity, making it particularly effective against a broad spectrum of weed species. Additionally, its chemical properties contribute to the development of formulations

This chemical is primarily utilized in the agricultural sector as a key intermediate in the synthesis of advanced herbicides. Its structure allows it to act as a building block for creating compounds that effectively target and control the growth of unwanted weeds in crops. The presence of the trifluoromethyl group enhances the herbicidal activity, making it particularly effective against a broad spectrum of weed species. Additionally, its chemical properties contribute to the development of formulations that are stable and efficient under various environmental conditions, ensuring prolonged efficacy in the field. Researchers also explore its potential in developing new agrochemicals with improved safety profiles and reduced environmental impact.

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