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Structure of 904885-87-6
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2-Formylquinoline-6-carboxylic acid features a dual functional group architecture with an aldehyde and carboxylic acid positioned ortho to each other on a quinoline scaffold. This arrangement enables direct coupling or cyclization reactions in synthetic pathways. The molecule exhibits enhanced solubility in polar solvents and stability under standard bench conditions, facilitating its use in transition metal-catalyzed transformations and heterocyclic scaffold elaboration.
2-Formylquinoline-6-carboxylic acid serves as a versatile bifunctional building block in medicinal chemistry and materials science, enabling direct incorporation into heterocyclic scaffolds via condensation, cyclization, or cross-coupling reactions. The ortho-positioned aldehyde and carboxylic acid groups exhibit complementary reactivity, facilitating efficient derivatization under standard conditions. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for iterative synthesis campaigns requiring functional group compatibility and structural precision.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: