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Structure of 1442437-21-9
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This dihydropyridazine derivative features a hydroxyl group at C4 and a ketone at C6, paired with a carboxylic acid at C3. The scaffold delivers high functional group compatibility for conjugation, enabling integration into bioactive molecules under standard conditions.
4-Hydroxy-6-oxo-1,6-dihydropyridazine-3-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling access to pyridazine-based scaffolds relevant in medicinal chemistry. Its orthogonally functionalized core—combining a hydroxyl group, ketone, and carboxylic acid—facilitates diverse transformations including amidation, esterification, and cyclization. The compound exhibits bench stability and compatibility with standard purification techniques, supporting efficient integration into multi-step synthetic sequences.
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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: