2-Bromo-4-nitro-1-naphthalenamine

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Reagent Code: #151095
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CAS Number 63240-26-6

science Other reagents with same CAS 63240-26-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.08 g/mol
Formula C₁₀H₇BrN₂O₂
badge Registry Numbers
MDL Number MFCD00085870
thermostat Physical Properties
Melting Point 250 °C
Boiling Point 436.0±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.735±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 for producing azo dyes that exhibit strong color fastness. It also serves in the preparation of fluorescent whitening agents for textiles and paper. Additionally, it finds application in the development of certain pharmaceuticals and agrochemicals due to its reactive functional groups, which allow for further chemical modifications. Its nitro and amine groups enable coupling reactions useful in organic synthesis and research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,630.00
inventory 250mg
10-20 days ฿2,080.00
inventory 1g
10-20 days ฿4,830.00

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2-Bromo-4-nitro-1-naphthalenamine
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Used as an intermediate in the synthesis of dyes and pigments, particularly for producing azo dyes that exhibit strong color fastness. It also serves in the preparation of fluorescent whitening agents for textiles and paper. Additionally, it finds application in the development of certain pharmaceuticals and agrochemicals due to its reactive functional groups, which allow for further chemical modifications. Its nitro and amine groups enable coupling reactions useful in organic synthesis and research.

Used as an intermediate in the synthesis of dyes and pigments, particularly for producing azo dyes that exhibit strong color fastness. It also serves in the preparation of fluorescent whitening agents for textiles and paper. Additionally, it finds application in the development of certain pharmaceuticals and agrochemicals due to its reactive functional groups, which allow for further chemical modifications. Its nitro and amine groups enable coupling reactions useful in organic synthesis and research.

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