2-Methoxy-3-nitrobenzamide

≥95%

Reagent Code: #203731
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CAS Number 722538-98-9

science Other reagents with same CAS 722538-98-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.1601 g/mol
Formula C₈H₈N₂O₄
badge Registry Numbers
MDL Number MFCD18398355
thermostat Physical Properties
Melting Point 124 °C
Boiling Point 326.5±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.362±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and agrochemicals. Its functional groups—methoxy, nitro, and amide—allow for selective transformations, making it valuable in constructing complex molecules. The nitro group can be reduced to an amine, enabling further derivatization such as diazotization or amide coupling. The presence of the methoxy group influences reactivity and regioselectivity in electrophilic substitution reactions. It is also employed in the development of bioactive compounds, including potential antimicrobial or anti-inflammatory agents, due to its structural similarity to known pharmacophores. In research settings, it serves as a building block for heterocyclic synthesis, particularly in the formation of fused ring systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,200.00
inventory 5g
10-20 days ฿9,600.00
inventory 10g
10-20 days ฿16,000.00
inventory 25g
10-20 days ฿32,000.00

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2-Methoxy-3-nitrobenzamide
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Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and agrochemicals. Its functional groups—methoxy, nitro, and amide—allow for selective transformations, making it valuable in constructing complex molecules. The nitro group can be reduced to an amine, enabling further derivatization such as diazotization or amide coupling. The presence of the methoxy group influences reactivity and regioselectivity in electrophilic substitution reactions. It is also employed in the development of bioactive compounds, including potential antimicrobial or anti-inflammatory agents, due to its structural similarity to known pharmacophores. In research settings, it serves as a building block for heterocyclic synthesis, particularly in the formation of fused ring systems.
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