Methyl 3-Methoxy-4-Nitrobenzoate

≥95%

Reagent Code: #207628
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CAS Number 5081-37-8

science Other reagents with same CAS 5081-37-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.17 g/mol
Formula C₉H₉NO₅
badge Registry Numbers
MDL Number MFCD00051967
thermostat Physical Properties
Melting Point 86-88°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its nitro and methoxy functional groups allow for selective reductions and substitutions, making it valuable in constructing complex aromatic molecules. Commonly employed in the development of active ingredients in crop protection agents and in the synthesis of dyes and specialty chemicals. The ester group facilitates further derivatization, enabling its use in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,240.00
inventory 5g
10-20 days ฿6,470.00
inventory 10g
10-20 days ฿11,680.00

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Methyl 3-Methoxy-4-Nitrobenzoate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its nitro and methoxy functional groups allow for selective reductions and substitutions, making it valuable in constructing complex aromatic molecules. Commonly employed in the development of active ingredients in crop protection agents and in the synthesis of dyes and specialty chemicals. The ester group facilitates further derivatization, enabling its use in multi-step synthetic routes.<

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its nitro and methoxy functional groups allow for selective reductions and substitutions, making it valuable in constructing complex aromatic molecules. Commonly employed in the development of active ingredients in crop protection agents and in the synthesis of dyes and specialty chemicals. The ester group facilitates further derivatization, enabling its use in multi-step synthetic routes.

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