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Structure of 31930-18-4
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2-Amino-4-nitrobenzamide features a strategically positioned amino group and nitro substituent on the benzamide scaffold, enabling selective conjugation in synthetic peptide analogs. This electron-deficient aromatic core facilitates efficient coupling reactions under mild conditions, while the amide functionality enhances solubility and metabolic stability in bioconjugation workflows.
2-Amino-4-nitrobenzamide serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling efficient access to substituted quinazolines and other nitrogen-containing scaffolds. Its dual functionality—amine and nitro groups—facilitates sequential transformations, including selective reduction, coupling reactions, and cyclization protocols. The compound exhibits good bench stability and is amenable to standard purification methods, making it well-suited for iterative synthetic workflows in API development and process chemistry.
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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: