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Structure of 73568-35-1
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6-Bromo-2-chloroquinoline-3-carbaldehyde features a sterically accessible aldehyde handle flanked by electron-deficient halogens, enabling direct coupling in transition-metal-catalyzed transformations. The quinoline scaffold provides rigidity and enhanced solubility in organic media, facilitating use in medicinal chemistry and materials synthesis under standard conditions.
6-Bromo-2-chloroquinoline-3-carbaldehyde serves as a versatile building block in the synthesis of functionalized quinoline scaffolds. Its bromo and chloro substituents enable palladium-catalyzed cross-coupling reactions, while the aldehyde group facilitates condensation, reductive amination, or nucleophilic addition pathways. The molecule exhibits good bench stability and is readily purified by column chromatography, making it well-suited for iterative synthetic sequences in 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 : H302-H319
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: