2,6-Dichloro-3-methoxyaniline

95%

Reagent Code: #177437
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CAS Number 55285-43-3

science Other reagents with same CAS 55285-43-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.04 g/mol
Formula C₇H₇Cl₂NO
badge Registry Numbers
MDL Number MFCD20694612
thermostat Physical Properties
Boiling Point 269.7±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.375±0.06 g/cm3(Predicted)
Storage 2-8°C, preserved from light, dry sealed

description Product Description

Used as an intermediate in the synthesis of agrochemicals and dyes, including azo dyes for textiles and printing inks. Plays a key role in the production of certain herbicides and fungicides due to its reactive amine group and halogen substituents. Also employed in the development of specialty chemicals for polymer stabilization and in the preparation of complex organic molecules requiring selective substitution patterns. Its methoxy and chlorine groups allow for controlled reactivity in coupling reactions and heterocycle formation.

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inventory 100mg
10-20 days ฿2,560.00

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2,6-Dichloro-3-methoxyaniline
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Used as an intermediate in the synthesis of agrochemicals and dyes, including azo dyes for textiles and printing inks. Plays a key role in the production of certain herbicides and fungicides due to its reactive amine group and halogen substituents. Also employed in the development of specialty chemicals for polymer stabilization and in the preparation of complex organic molecules requiring selective substitution patterns. Its methoxy and chlorine groups allow for controlled reactivity in coupling reactio

Used as an intermediate in the synthesis of agrochemicals and dyes, including azo dyes for textiles and printing inks. Plays a key role in the production of certain herbicides and fungicides due to its reactive amine group and halogen substituents. Also employed in the development of specialty chemicals for polymer stabilization and in the preparation of complex organic molecules requiring selective substitution patterns. Its methoxy and chlorine groups allow for controlled reactivity in coupling reactions and heterocycle formation.

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