2-(4-Nitrophenyl)ethyl Bromide

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Reagent Code: #217135
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CAS Number 5339-26-4

science Other reagents with same CAS 5339-26-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.06 g/mol
Formula C₈H₈BrNO₂
badge Registry Numbers
MDL Number MFCD00007386
thermostat Physical Properties
Melting Point 67-69°C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and fine chemicals. Its reactivity as an alkylating agent makes it valuable for introducing the 2-(4-nitrophenyl)ethyl group into target molecules. The nitro group allows for further functionalization, such as reduction to an amine, enabling the construction of more complex structures like active pharmaceutical ingredients. It is also employed in the synthesis of certain dyes and fluorescent probes due to the aromatic nitro moiety’s electronic properties. Commonly used in research settings for developing new bioactive compounds.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿590.00
inventory 100g
10-20 days ฿2,160.00
inventory 500g
10-20 days ฿10,680.00

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2-(4-Nitrophenyl)ethyl Bromide
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Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and fine chemicals. Its reactivity as an alkylating agent makes it valuable for introducing the 2-(4-nitrophenyl)ethyl group into target molecules. The nitro group allows for further functionalization, such as reduction to an amine, enabling the construction of more complex structures like active pharmaceutical ingredients. It is also employed in the synthesis of certain dyes and fluorescent probes du

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and fine chemicals. Its reactivity as an alkylating agent makes it valuable for introducing the 2-(4-nitrophenyl)ethyl group into target molecules. The nitro group allows for further functionalization, such as reduction to an amine, enabling the construction of more complex structures like active pharmaceutical ingredients. It is also employed in the synthesis of certain dyes and fluorescent probes due to the aromatic nitro moiety’s electronic properties. Commonly used in research settings for developing new bioactive compounds.

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