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Structure of 841296-15-9
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Methyl 4-amino-3-formylbenzoate features a formyl group flanked by electron-rich amino and ester functionalities, enabling direct integration into multistep syntheses. This bench-stable scaffold supports efficient derivatization in medicinal chemistry and materials development under standard conditions.
Methyl 4-amino-3-formylbenzoate serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling efficient access to substituted benzimidazoles, quinoline derivatives, and other heterocyclic scaffolds. The formyl group facilitates nucleophilic addition reactions, while the amino and ester functionalities offer orthogonal reactivity for sequential transformations. Its bench-stable nature and compatibility with standard coupling and cyclization protocols make it well-suited for multi-step synthesis and process-scale applications.
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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: