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Structure of 261768-25-6
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This pyridazinone-acetic acid derivative integrates a reactive ketone and carboxylic acid functional group, enabling direct conjugation or derivatization in synthetic workflows. The electron-deficient pyridazinone core enhances stability under standard conditions, while the pendant acetyl moiety facilitates modular assembly in bioconjugation and medicinal chemistry applications.
2-(6-Oxo-1,6-dihydropyridazin-3-yl)acetic acid serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridazinone-based heterocyclic scaffolds. Its α-acyl functionality facilitates nucleophilic substitution and condensation reactions, while the carboxylic acid group supports direct derivatization or salt formation. The compound exhibits good bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis campaigns in API development.
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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: