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Structure of 2411793-14-9
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6-Bromo-N,N-bis(4-methoxybenzyl)-4-methyl-5-(trifluoromethyl)pyridin-2-amine features a sterically hindered pyridine core with electron-withdrawing trifluoromethyl and bromo substituents, enabling precise coupling in late-stage functionalization. The bis(4-methoxybenzyl) amine moiety enhances solubility and stability under standard conditions, while the methyl group provides a strategic handle for further derivatization in medicinal chemistry campaigns.
6-Bromo-N,N-bis(4-methoxybenzyl)-4-methyl-5-(trifluoromethyl)pyridin-2-amine serves as a versatile building block for late-stage functionalization in medicinal chemistry. The bromine at the 6-position enables palladium-catalyzed cross-coupling reactions, while the trifluoromethyl group enhances metabolic stability and lipophilicity. The bis(4-methoxybenzyl) protection offers robust orthogonality and ease of purification, with the methyl substituent providing steric control during subsequent transformations.
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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: