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Structure of 6284-92-0
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3-Hydroxy-4-methoxy-2-nitrobenzaldehyde features a strategically positioned aldehyde group flanked by electron-withdrawing nitro and electron-donating methoxy functionalities, enabling precise tuning of reactivity in coupling reactions. The phenolic hydroxyl enhances solubility and facilitates derivatization, while the ortho-nitro substituent stabilizes intermediates under standard conditions. This scaffold serves as a key building block for bioactive heterocycles and fluorescent probes.
3-Hydroxy-4-methoxy-2-nitrobenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling the construction of bioactive heterocycles and functionalized aromatic scaffolds. Its ortho-hydroxyl and methoxy groups provide complementary reactivity for electrophilic substitution and metal-catalyzed coupling reactions, while the nitro and aldehyde functionalities offer robust handles for sequential transformations. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis in medicinal chemistry and materials 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: