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Structure of 1402401-43-7
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This dihydropyrimidine derivative features a reactive aldehyde group flanked by an amino functionality and a ketone, enabling direct coupling in heterocyclic synthesis. The scaffold supports rapid derivatization under mild conditions, serving as a key intermediate in the construction of biologically active pyrimidine analogs.
2-Amino-6-oxo-1,6-dihydropyrimidine-5-carbaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds. Its dual functionality—amino and aldehyde groups—facilitates sequential transformations, including reductive amination, condensation reactions, and cyclization protocols. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it valuable for medicinal chemistry campaigns and process-scale synthesis of bioactive molecules.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: