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Structure of 5344-49-0
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2-Chloro-6-nitrobenzoic acid features a strategically positioned nitro group and chlorine substituent on the aromatic ring, delivering enhanced electrophilicity for downstream coupling reactions. This electron-deficient scaffold integrates readily into pharmaceutical intermediates and functional materials under standard conditions.
2-Chloro-6-nitrobenzoic acid serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient functionalization at the aromatic ring through nucleophilic substitution or transition-metal-catalyzed coupling. The ortho-chloro and para-nitro groups provide orthogonal reactivity, facilitating sequential transformations while maintaining stability under standard bench conditions. Its well-defined reactivity profile supports reliable access to substituted heterocycles and complex scaffolds.
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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: