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Structure of 178686-24-3
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3-Ethoxy-4-hydroxy-5-nitrobenzaldehyde features a conjugated aldehyde group flanked by electron-withdrawing nitro and hydroxyl functionalities, enabling selective coupling reactions. The ethoxy substituent enhances solubility in organic solvents while maintaining stability under standard bench conditions. This trifunctional scaffold supports modular synthesis of bioactive heterocycles and functionalized aromatic systems.
3-Ethoxy-4-hydroxy-5-nitrobenzaldehyde serves as a versatile building block for the synthesis of functionalized heterocycles and bioactive scaffolds. Its ortho-hydroxy and para-nitro substituents enable facile cyclization reactions, while the aldehyde group supports efficient condensation and reductive amination protocols. The ethoxy group enhances solubility and provides a handle for further derivatization. This compound exhibits bench stability and is compatible with standard purification methods, making it suitable for iterative synthesis in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: