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Structure of 72407-17-1
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2,4-Dichloro-6,7-dimethoxyquinoline features a sterically hindered quinoline core with electron-donating methoxy groups flanking a chlorine-substituted heterocyclic scaffold. This configuration enhances stability and enables selective coupling in transition-metal-catalyzed transformations. The molecule integrates readily into advanced synthetic intermediates for pharmaceutical and agrochemical development under standard conditions.
2,4-Dichloro-6,7-dimethoxyquinoline serves as a versatile building block in medicinal chemistry, enabling efficient construction of quinoline-based scaffolds through palladium-catalyzed cross-coupling reactions. The dichloro substitution pattern facilitates sequential functionalization, while the dimethoxy groups provide enhanced solubility and stability under standard reaction conditions. Its bench-stable nature and compatibility with diverse coupling partners make it ideal for modular synthesis of bioactive molecules and pharmaceutical intermediates.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: