1-(3-Bromopropoxy)-4-nitrobenzene

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Reagent Code: #150217
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CAS Number 13094-50-3

science Other reagents with same CAS 13094-50-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.08 g/mol
Formula C₉H₁₀BrNO₃
badge Registry Numbers
MDL Number MFCD00596643
thermostat Physical Properties
Melting Point 56-58 °C
Boiling Point 373.3 °C(Predicted)
inventory_2 Storage & Handling
Density 1.6737 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its nitro group allows for further functionalization, such as reduction to an amine, enabling the construction of more complex molecules. The bromopropoxy chain acts as a linker, making it useful in the development of functionalized aromatic compounds for use in medicinal chemistry and materials science. Commonly employed in reactions involving nucleophilic substitution due to the reactive bromide moiety.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,720.00
inventory 1g
10-20 days ฿4,430.00
inventory 5g
10-20 days ฿12,860.00
inventory 25g
10-20 days ฿38,580.00

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1-(3-Bromopropoxy)-4-nitrobenzene
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its nitro group allows for further functionalization, such as reduction to an amine, enabling the construction of more complex molecules. The bromopropoxy chain acts as a linker, making it useful in the development of functionalized aromatic compounds for use in medicinal chemistry and materials science. Commonly employed in reactions involving nucleophilic substitution due to the reactive

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its nitro group allows for further functionalization, such as reduction to an amine, enabling the construction of more complex molecules. The bromopropoxy chain acts as a linker, making it useful in the development of functionalized aromatic compounds for use in medicinal chemistry and materials science. Commonly employed in reactions involving nucleophilic substitution due to the reactive bromide moiety.

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