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Structure of 320349-89-1
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This quinoline-based carboxylic acid features a ketone at the 2-position and a carboxyl group at the 7-position, creating a rigid, electron-deficient scaffold. The conjugated system enables direct integration into heterocyclic synthesis, while the acidic functionality supports salt formation and derivatization under standard conditions.
2-Oxo-1,2-dihydroquinoline-7-carboxylic acid serves as a versatile scaffold for heterocyclic synthesis, enabling efficient access to quinoline-based pharmacophores. Its carboxylic acid functionality facilitates direct derivatization and conjugation, while the enone system supports Michael addition and cycloaddition reactions. Bench-stable and compatible with standard purification methods, it functions effectively in multi-step synthetic sequences targeting bioactive molecules.
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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: