N-(4-Bromophenyl)-2-nitroaniline

95%

Reagent Code: #219211
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CAS Number 58476-59-8

science Other reagents with same CAS 58476-59-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.12 g/mol
Formula C₁₂H₉BrN₂O₂
badge Registry Numbers
MDL Number MFCD00092900
thermostat Physical Properties
Melting Point 162 °C
Boiling Point 393.1±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.597±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof storage, dry seal

description Product Description

Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes which are valued for their color intensity and stability. It also serves in the development of certain pharmaceuticals and agrochemicals due to its aromatic and nitro-functionalized structure, which can be further modified in multi-step reactions. Additionally, it finds use in research laboratories for the preparation of more complex organic molecules, especially in reactions involving nitro group reduction or nucleophilic aromatic substitution.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,170.00
inventory 250mg
10-20 days ฿2,900.00
inventory 1g
10-20 days ฿11,570.00

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N-(4-Bromophenyl)-2-nitroaniline
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Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes which are valued for their color intensity and stability. It also serves in the development of certain pharmaceuticals and agrochemicals due to its aromatic and nitro-functionalized structure, which can be further modified in multi-step reactions. Additionally, it finds use in research laboratories for the preparation of more complex organic molecules, especially in reactions involving nitro group re

Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes which are valued for their color intensity and stability. It also serves in the development of certain pharmaceuticals and agrochemicals due to its aromatic and nitro-functionalized structure, which can be further modified in multi-step reactions. Additionally, it finds use in research laboratories for the preparation of more complex organic molecules, especially in reactions involving nitro group reduction or nucleophilic aromatic substitution.

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