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Structure of 1112193-37-9
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This pyridooxazine scaffold delivers a rigid, electron-rich heterocyclic framework ideal for medicinal chemistry applications. Featuring a fused bicyclic structure with defined stereochemistry, it integrates readily into molecular architectures requiring enhanced metabolic stability and improved membrane permeability.
2,3-Dihydro-1H-pyrido[2,3-b][1,4]oxazine serves as a versatile heterocyclic scaffold in medicinal chemistry, enabling efficient construction of bioactive molecules through standard functionalization protocols. Its fused ring system exhibits bench stability and compatibility with diverse reaction conditions, facilitating downstream modifications such as C–H arylation and N-alkylation. The structure functions as a privileged core in the synthesis of kinase inhibitors and CNS-targeted compounds, offering predictable reactivity and favorable purification profiles in multi-step 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: