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Structure of 20348-23-6
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This heterocyclic scaffold features a fused pyridine-oxazine core with inherent stability and tunable reactivity. The saturated dihydropyridine ring enables selective functionalization, while the oxygen atom enhances polarity and solubility. This structure serves as a key building block in medicinal chemistry for accessing bioactive molecules through modular derivatization pathways.
3,4-Dihydro-2H-pyrido[3,2-b][1,4]oxazine serves as a versatile heterocyclic scaffold in medicinal chemistry, enabling efficient construction of bioactive molecules through standard functionalization at the pyridine and oxazine rings. Its stability under routine reaction conditions and compatibility with common coupling and reduction protocols facilitate downstream derivatization. Functions as a key building block for CNS-targeted compounds and kinase inhibitors, offering predictable reactivity in transition-metal-catalyzed transformations.
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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: