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Structure of 31680-08-7
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4-Methoxy-3-nitrobenzaldehyde features a para-substituted electron-deficient aromatic ring, integrating a methoxy group and a nitro functionality flanking the aldehyde. This combination enables selective reactivity in cross-coupling and condensation reactions, offering enhanced solubility and stability under standard conditions.
4-Methoxy-3-nitrobenzaldehyde serves as a versatile building block in medicinal chemistry and materials science, enabling efficient access to functionalized aromatic scaffolds. Its ortho-directed electrophilic substitution pattern and complementary reactivity of the aldehyde and nitro groups facilitate sequential transformations. The methoxy substituent enhances solubility and modulates electronic effects, while the aldehyde group enables facile imine formation, reductive amination, and coupling reactions. This compound offers bench stability and straightforward purification, making it well-suited for iterative synthesis workflows and scale-up applications.
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Lot numbers can be found on the outside label of a product: