1-(Methoxymethyl)-4-nitrobenzene

≥95%

Reagent Code: #213185
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CAS Number 1515-83-9

science Other reagents with same CAS 1515-83-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.16 g/mol
Formula C₈H₉NO₃
badge Registry Numbers
MDL Number MFCD00024782
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its nitro group can be reduced to an amine, enabling the formation of amino derivatives important in dye and drug manufacturing. The methoxymethyl group acts as a protecting group for alcohols in multi-step syntheses, making it valuable in the production of complex molecules. Also employed in the development of specialty chemicals where controlled reactivity and functional group transformation are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,790.00
inventory 1g
10-20 days ฿5,040.00
inventory 5g
10-20 days ฿20,570.00

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1-(Methoxymethyl)-4-nitrobenzene
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its nitro group can be reduced to an amine, enabling the formation of amino derivatives important in dye and drug manufacturing. The methoxymethyl group acts as a protecting group for alcohols in multi-step syntheses, making it valuable in the production of complex molecules. Also employed in the development of specialty chemicals where controlled reactivity and functional group transformat

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its nitro group can be reduced to an amine, enabling the formation of amino derivatives important in dye and drug manufacturing. The methoxymethyl group acts as a protecting group for alcohols in multi-step syntheses, making it valuable in the production of complex molecules. Also employed in the development of specialty chemicals where controlled reactivity and functional group transformation are required.

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