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Structure of 2599846-40-7
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4-(2,4-Dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid features a conjugated pyrimidinone core linked to a benzoic acid moiety, enabling integration into bioactive scaffolds. The electron-deficient heterocycle pairs with the carboxylic acid group to facilitate coupling reactions and enhance solubility in polar media. This structure supports applications in medicinal chemistry and molecular probe development.
4-(2,4-Dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds via condensation and cyclization reactions. Its dual functionality—carboxylic acid and 2,4-dioxotetrahydropyrimidine moiety—facilitates diverse transformations under mild conditions, with excellent bench stability and straightforward purification. Functions effectively in solid-phase and solution-phase workflows for medicinal chemistry campaigns requiring modular pyrimidine integration.
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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: