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Structure of 619-17-0
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2-Amino-4-nitrobenzoic acid features a strategically positioned amino group and electron-deficient nitro moiety on a benzoic acid scaffold, enabling direct incorporation into conjugated systems. This dual-functional architecture supports efficient coupling reactions under standard conditions, delivering stable intermediates for pharmaceutical and materials applications.
2-Amino-4-nitrobenzoic acid serves as a versatile building block in synthetic organic chemistry, enabling access to substituted benzimidazoles, quinoline derivatives, and other heterocyclic scaffolds through well-established coupling and cyclization protocols. Its complementary functional groups—amine and nitro—support sequential transformations with high chemoselectivity, while the carboxylic acid facilitates derivatization or salt formation for improved handling and purification. The compound exhibits good bench stability and is readily employed in medicinal chemistry campaigns targeting kinase inhibitors and antimicrobial agents.
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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: