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Structure of 4113-97-7
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This pyrimidinone-acetic acid derivative integrates a reactive acetic acid handle with a stable dihydropyrimidinone core, enabling efficient conjugation in bioconjugation workflows. The electron-deficient heterocycle enhances reactivity while maintaining bench-stable handling under standard conditions.
2-(2,4-Dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetic acid serves as a versatile building block for pyrimidine-based heterocycles, enabling efficient access to pharmaceutically relevant scaffolds. Its malonic ester-like reactivity facilitates condensation with amines and hydrazines under mild conditions, offering high functional group tolerance and ease of purification. The molecule's bench stability and compatibility with standard coupling protocols make it ideal for medicinal chemistry campaigns and API intermediate synthesis.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: