1-Bromo-2-nitronaphthalene

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Reagent Code: #148989
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CAS Number 4185-55-1

science Other reagents with same CAS 4185-55-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.06 g/mol
Formula C₁₀H₆BrNO₂
badge Registry Numbers
MDL Number MFCD00971807
thermostat Physical Properties
Melting Point 98-99 °C
Boiling Point 338.1±15.0 °C
inventory_2 Storage & Handling
Density 1.662±0.06 g/cm3
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of naphthol-based azo dyes. It plays a role in the development of organic semiconductors due to its electron-withdrawing properties when incorporated into larger conjugated systems. Also utilized in the preparation of fluorescent brightening agents for textiles and paper. Its reactivity allows for substitution reactions in pharmaceutical research, especially in the construction of nitrogen-containing heterocycles. Limited use in agrochemicals as a building block for certain plant growth regulators.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,250.00
inventory 250mg
10-20 days ฿2,560.00
inventory 1g
10-20 days ฿5,280.00
inventory 5g
10-20 days ฿15,040.00
inventory 10g
10-20 days ฿30,070.00

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1-Bromo-2-nitronaphthalene
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Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of naphthol-based azo dyes. It plays a role in the development of organic semiconductors due to its electron-withdrawing properties when incorporated into larger conjugated systems. Also utilized in the preparation of fluorescent brightening agents for textiles and paper. Its reactivity allows for substitution reactions in pharmaceutical research, especially in the construction of nitrogen-containing heterocycle

Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of naphthol-based azo dyes. It plays a role in the development of organic semiconductors due to its electron-withdrawing properties when incorporated into larger conjugated systems. Also utilized in the preparation of fluorescent brightening agents for textiles and paper. Its reactivity allows for substitution reactions in pharmaceutical research, especially in the construction of nitrogen-containing heterocycles. Limited use in agrochemicals as a building block for certain plant growth regulators.

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