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Structure of 20146-25-2
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This furan-quinoline hybrid delivers a rigid, planar scaffold with enhanced π-conjugation, enabling efficient integration into functional materials. The carboxylic acid group facilitates direct coupling reactions and enables solubility tuning in polar solvents.
2-Furan-2-yl-quinoline-4-carboxylic acid serves as a versatile building block in the synthesis of bioactive heterocycles, enabling efficient construction of fused polycyclic scaffolds. Its carboxylic acid functionality facilitates direct coupling reactions, while the quinoline and furan moieties provide orthogonal reactivity for downstream functionalization. The compound exhibits good bench stability and is compatible with standard amide coupling and Suzuki-Miyaura protocols, making it well-suited for medicinal chemistry and materials science applications.
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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 : 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: