5-Bromo-4-methoxy-2-nitroaniline

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Reagent Code: #49015
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CAS Number 6943-69-7

science Other reagents with same CAS 6943-69-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.0461 g/mol
Formula C₇H₇BrN₂O₃
badge Registry Numbers
MDL Number MFCD00031127
thermostat Physical Properties
Boiling Point 374.6 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.718g/cm3
Storage room temperature

description Product Description

Used primarily as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes, which are widely applied in textiles, inks, and plastics. Its nitro and amino groups make it a valuable building block for creating complex organic compounds. Additionally, it finds use in the development of pharmaceuticals and agrochemicals, where it serves as a precursor for active ingredients. Its bromo and methoxy substituents enhance its reactivity, making it suitable for selective chemical transformations in organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,061.00

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5-Bromo-4-methoxy-2-nitroaniline
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Used primarily as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes, which are widely applied in textiles, inks, and plastics. Its nitro and amino groups make it a valuable building block for creating complex organic compounds. Additionally, it finds use in the development of pharmaceuticals and agrochemicals, where it serves as a precursor for active ingredients. Its bromo and methoxy substituents enhance its reactivity, making it suitable for selective ch

Used primarily as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes, which are widely applied in textiles, inks, and plastics. Its nitro and amino groups make it a valuable building block for creating complex organic compounds. Additionally, it finds use in the development of pharmaceuticals and agrochemicals, where it serves as a precursor for active ingredients. Its bromo and methoxy substituents enhance its reactivity, making it suitable for selective chemical transformations in organic synthesis.

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