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Structure of 944401-56-3
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5-Bromo-4-(trifluoromethyl)pyridin-2-amine features a bromine atom at the 5-position and a trifluoromethyl group at the 4-position of the pyridine ring, creating a highly electron-deficient heterocyclic scaffold. This configuration enables efficient cross-coupling reactions in medicinal chemistry and materials synthesis. The amine functionality provides a reactive handle for further derivatization under mild conditions.
5-Bromo-4-(trifluoromethyl)pyridin-2-amine serves as a versatile building block in medicinal chemistry and catalytic cross-coupling reactions. The bromo group enables palladium-catalyzed coupling with boronic acids, while the trifluoromethyl moiety enhances metabolic stability and lipophilicity. Its pyridine amine functionality provides a handle for further derivatization, including amidation or electrophilic substitution. The compound exhibits good bench stability and facilitates efficient purification, making it well-suited for iterative synthesis of complex heterocyclic scaffolds.
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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-H319
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: