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Structure of 70639-77-9
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This tetrahydroquinoline derivative features a fused bicyclic core with a carboxylic acid at the 6-position and a ketone at the 2-position, enabling direct integration into bioactive molecule scaffolds. The electron-deficient quinoline ring facilitates nucleophilic addition reactions, while the carboxylic acid group supports conjugation via amide or ester linkages under standard conditions.
2-Oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid serves as a versatile scaffold for medicinal chemistry and heterocyclic synthesis, enabling efficient access to quinoline-based pharmacophores. Its carboxylic acid functionality facilitates derivatization via amide coupling, esterification, or decarboxylation protocols. The molecule exhibits bench stability and tolerates common functional groups, supporting its use in modular library construction and targeted synthesis of bioactive compounds.
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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: