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Structure of 156699-39-7
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(S)-Tetrahydropyridazine-1,2,3-tricarboxylic acid 1,2-di-tert-butyl ester features a stereochemically defined tetrahydropyridazine core bearing three carboxylic acid ester functionalities. The di-tert-butyl protection imparts enhanced stability and solubility in organic solvents, enabling straightforward handling and compatibility with multi-step synthetic sequences. This derivative serves as a key building block for the synthesis of bioactive heterocycles and peptidomimetics.
(S)-Tetrahydropyridazine-1,2,3-tricarboxylic acid 1,2-di-tert-butyl ester serves as a versatile chiral building block for the synthesis of nitrogen-rich heterocyclic scaffolds. The di-tert-butyl ester protection offers enhanced bench stability and facilitates purification, while the tetrahydropyridazine core enables selective functionalization at multiple positions. This compound functions as a key intermediate in the construction of biologically relevant frameworks, particularly in medicinal chemistry campaigns requiring stereocontrolled access to saturated pyridazine derivatives.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P501
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Lot numbers can be found on the outside label of a product: