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Structure of 134997-87-8
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This oxazine carboxylic acid features a fused heterocyclic core with orthogonal functional groups enabling direct integration into medicinal chemistry scaffolds. The electron-deficient ring system supports selective derivatization, while the carboxylic acid moiety provides a handle for conjugation under standard coupling conditions.
3-Oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-6-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry campaigns, enabling access to bioactive scaffolds via standard functionalization protocols. Its fused oxazine core exhibits bench stability and tolerates diverse reaction conditions, facilitating coupling, derivatization, and cyclization steps in multistep synthesis. The carboxylic acid group provides a handle for amide formation and conjugation, while the ketone functionality supports nucleophilic addition and condensation reactions. This compound functions effectively in both solution-phase and solid-phase synthetic workflows.
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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: