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Structure of 18436-71-0
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4-Chloro-6-methylquinoline is a heterocyclic scaffold featuring a chlorine substituent at the 4-position and a methyl group at the 6-position on the quinoline core. This configuration imparts enhanced electron-withdrawing character and steric influence, enabling its use in transition metal-catalyzed coupling reactions. The compound exhibits good stability under standard bench conditions and demonstrates favorable solubility in common organic solvents, facilitating integration into synthetic workflows for pharmaceutical intermediates and functional materials.
4-Chloro-6-methylquinoline serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C4 position via palladium-catalyzed cross-coupling reactions. Its methyl group at C6 enhances lipophilicity and metabolic stability, while the chloro substituent provides a reliable handle for late-stage diversification. The scaffold exhibits excellent bench stability and compatibility with standard purification methods, facilitating efficient synthesis of quinoline-based drug candidates and kinase inhibitors.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-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: