(4,6-dichloro-m-phenylenedioxy)-di-acetic acid dimethyl ester

95%

Reagent Code: #168080
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CAS Number 262861-52-9

science Other reagents with same CAS 262861-52-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.13 g/mol
Formula C₁₂H₁₂Cl₂O₆
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of herbicidal compounds, particularly in the production of aryloxyphenoxypropionate class herbicides. These herbicides are effective against grass weeds in broadleaf crops. The compound's chlorinated aromatic structure and ester functionality make it suitable for further chemical modifications, enabling the development of active ingredients that inhibit acetyl-CoA carboxylase (ACCase) in target plants. Its role as a building block allows for efficient coupling reactions to form larger molecules with enhanced herbicidal activity and selectivity.

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inventory 1g
10-20 days ฿22,000.00

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(4,6-dichloro-m-phenylenedioxy)-di-acetic acid dimethyl ester
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Used as a key intermediate in the synthesis of herbicidal compounds, particularly in the production of aryloxyphenoxypropionate class herbicides. These herbicides are effective against grass weeds in broadleaf crops. The compound's chlorinated aromatic structure and ester functionality make it suitable for further chemical modifications, enabling the development of active ingredients that inhibit acetyl-CoA carboxylase (ACCase) in target plants. Its role as a building block allows for efficient coupling

Used as a key intermediate in the synthesis of herbicidal compounds, particularly in the production of aryloxyphenoxypropionate class herbicides. These herbicides are effective against grass weeds in broadleaf crops. The compound's chlorinated aromatic structure and ester functionality make it suitable for further chemical modifications, enabling the development of active ingredients that inhibit acetyl-CoA carboxylase (ACCase) in target plants. Its role as a building block allows for efficient coupling reactions to form larger molecules with enhanced herbicidal activity and selectivity.

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