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Structure of 1227585-56-9
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4-(Bromomethyl)-2-(trifluoromethyl)pyridine features a reactive bromomethyl group flanked by a strongly electron-withdrawing trifluoromethyl substituent, enabling efficient nucleophilic substitution and coupling reactions. The pyridine scaffold provides enhanced stability and solubility in polar organic media, facilitating its use in medicinal chemistry and materials synthesis.
4-(Bromomethyl)-2-(trifluoromethyl)pyridine serves as a versatile building block in medicinal chemistry, enabling efficient introduction of trifluoromethylated pyridyl moieties into target molecules. The bromomethyl group facilitates nucleophilic substitution and coupling reactions, while the trifluoromethyl substituent enhances metabolic stability and lipophilicity. Its bench-stable nature and compatibility with standard cross-coupling conditions make it ideal for constructing bioactive scaffolds and functionalized heterocycles.
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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#: 3265
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: