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Structure of 2417920-98-8
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6-Bromo-4-methyl-5-(trifluoromethyl)pyridin-2-amine features a trifluoromethyl group that enhances metabolic stability and electron deficiency, while the bromo and methyl substituents enable selective cross-coupling reactions. This pyridine scaffold serves as a key building block in pharmaceutical discovery, particularly for kinase inhibitors and bioactive heterocycles.
6-Bromo-4-methyl-5-(trifluoromethyl)pyridin-2-amine serves as a versatile building block in medicinal chemistry and catalytic cross-coupling reactions. Its bromine and amine functionalities enable sequential derivatization via Pd-catalyzed coupling, while the trifluoromethyl and methyl groups confer enhanced metabolic stability and modulated lipophilicity. The compound exhibits good bench stability and facilitates efficient access to complex heterocyclic scaffolds relevant to pharmaceutical development.
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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: