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Structure of 325486-45-1
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tert-Butyl 4-oxo-3,4-dihydropyridine-1(2H)-carboxylate features a reactive enolizable carbonyl adjacent to a dihydropyridine ring, enabling efficient functionalization in heterocyclic synthesis. This bench-stable, moisture-tolerant building block integrates readily into complex scaffolds via Michael additions and cycloadditions, offering a streamlined route to nitrogen-containing frameworks with high regiocontrol.
tert-Butyl 4-oxo-3,4-dihydropyridine-1(2H)-carboxylate serves as a versatile building block for pyridine-based heterocycles, enabling efficient access to substituted dihydropyridines and pyridines via standard reduction, alkylation, and cyclization protocols. Its tert-butyl ester group provides excellent bench stability and facilitates straightforward purification, while the 4-oxo functionality offers predictable reactivity in nucleophilic additions and condensation reactions. This compound functions reliably in multistep synthesis workflows requiring controlled functional group interconversions.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H319-H411
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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: