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Structure of 153775-42-9
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4-Cyano-3-nitrobenzoic acid features a conjugated triad of electron-withdrawing groups—cyano, nitro, and carboxylic acid—positioned ortho to one another, enhancing its utility in constructing electron-deficient scaffolds. This arrangement promotes strong intermolecular interactions and facilitates coupling reactions under mild conditions. The compound serves as a key building block for functionalized heterocycles, advanced materials, and bioactive molecule synthesis.
4-Cyano-3-nitrobenzoic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted quinoline and benzimidazole scaffolds. Its orthogonal functionality—cyano, nitro, and carboxylic acid groups—supports sequential transformations under standard conditions. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry campaigns 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: