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Structure of 346-55-4
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4-Chloro-7-trifluoromethylquinoline is a fluorinated quinoline derivative featuring a chloro group at the 4-position and a trifluoromethyl moiety at the 7-position. This electron-deficient scaffold enhances reactivity in transition-metal-catalyzed coupling reactions, offering improved solubility and stability under standard bench conditions.
4-Chloro-7-trifluoromethylquinoline serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive chloro substituent. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the quinoline core provides a rigid, planar scaffold suitable for target-directed synthesis. Bench-stable and readily purified by column chromatography, it facilitates efficient access to complex heterocyclic architectures in drug discovery programs.
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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-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: