Methyl 2-(4-nitrophenyl)acetate

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Reagent Code: #208836
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CAS Number 2945-08-6

science Other reagents with same CAS 2945-08-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.17 g/mol
Formula C₉H₉NO₄
badge Registry Numbers
MDL Number MFCD00024802
thermostat Physical Properties
Boiling Point 308.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

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. Commonly employed in the development of active ingredients in herbicides and in the synthesis of certain anti-inflammatory agents. Also utilized in research settings for the formation of heterocyclic compounds through cyclization reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿168.00
inventory 250mg
10-20 days ฿204.00
inventory 1g
10-20 days ฿348.00
inventory 5g
10-20 days ฿1,890.00
inventory 25g
10-20 days ฿6,790.00
inventory 100g
10-20 days ฿13,422.00

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Methyl 2-(4-nitrophenyl)acetate
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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. Commonly employed in the development of active ingredients in herbicides and in the synthesis of certain anti-inflammatory agents. Also utilized in research settings for the formation of heterocyclic compounds through cyclization reactions.

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. Commonly employed in the development of active ingredients in herbicides and in the synthesis of certain anti-inflammatory agents. Also utilized in research settings for the formation of heterocyclic compounds through cyclization reactions.

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