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Structure of 117519-13-8
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6-Chloro-2-(trifluoromethyl)pyridin-3-amine delivers a potent electron-deficient pyridine scaffold with orthogonal functional handles. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the chloro substituent enables palladium-catalyzed coupling reactions. This molecule serves as a key building block in medicinal chemistry for targeted kinase inhibitors and bioactive heterocycles.
6-Chloro-2-(trifluoromethyl)pyridin-3-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds via palladium-catalyzed cross-coupling reactions. The chloro group facilitates C–C and C–N bond formation under standard conditions, while the trifluoromethyl and amine functionalities offer enhanced metabolic stability and hydrogen-bonding capacity. Bench-stable and compatible with common protecting groups, it supports scalable synthesis of kinase inhibitors and other bioactive molecules.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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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: