2-Methoxy-3-nitrobenzaldehyde

95%

Reagent Code: #203683
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CAS Number 22065-49-2

science Other reagents with same CAS 22065-49-2

blur_circular Chemical Specifications

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Weight 181.15 g/mol
Formula C₈H₇NO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients that require substituted benzaldehyde derivatives. Its nitro and methoxy functional groups allow for selective reactions, making it valuable in creating complex organic molecules. Commonly employed in the preparation of dyes and fluorescent probes due to its ability to undergo condensation reactions. Also utilized in research settings for the development of sensors and optoelectronic materials where aromatic aldehydes with electron-withdrawing and electron-donating groups are needed.

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inventory 1g
10-20 days ฿22,500.00

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2-Methoxy-3-nitrobenzaldehyde
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients that require substituted benzaldehyde derivatives. Its nitro and methoxy functional groups allow for selective reactions, making it valuable in creating complex organic molecules. Commonly employed in the preparation of dyes and fluorescent probes due to its ability to undergo condensation reactions. Also utilized in research settings for the development of sensors and opto

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients that require substituted benzaldehyde derivatives. Its nitro and methoxy functional groups allow for selective reactions, making it valuable in creating complex organic molecules. Commonly employed in the preparation of dyes and fluorescent probes due to its ability to undergo condensation reactions. Also utilized in research settings for the development of sensors and optoelectronic materials where aromatic aldehydes with electron-withdrawing and electron-donating groups are needed.

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