1,3-Dichloro-2-methoxy-5-nitrobenzene

98%

Reagent Code: #170256
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CAS Number 17742-69-7

science Other reagents with same CAS 17742-69-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.02 g/mol
Formula C₇H₅Cl₂NO₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of agrochemicals and dyes, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions where nitro and chloro functionalities allow for further substitution and transformation. Its methoxy and nitro groups enhance reactivity in nucleophilic aromatic substitution, making it valuable in the development of complex aromatic compounds for crop protection agents. Also employed in research for designing novel bioactive molecules due to its electron-withdrawing group arrangement.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿174.00
5g
10-20 days ฿820.00
25g
10-20 days ฿1,952.50
1,3-Dichloro-2-methoxy-5-nitrobenzene
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Used as an intermediate in the synthesis of agrochemicals and dyes, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions where nitro and chloro functionalities allow for further substitution and transformation. Its methoxy and nitro groups enhance reactivity in nucleophilic aromatic substitution, making it valuable in the development of complex aromatic compounds for crop protection agents. Also employed in research for designing novel bioactive

Used as an intermediate in the synthesis of agrochemicals and dyes, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions where nitro and chloro functionalities allow for further substitution and transformation. Its methoxy and nitro groups enhance reactivity in nucleophilic aromatic substitution, making it valuable in the development of complex aromatic compounds for crop protection agents. Also employed in research for designing novel bioactive molecules due to its electron-withdrawing group arrangement.

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