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Structure of 956104-42-0
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2-Bromo-5-nitro-3-(trifluoromethyl)pyridine features a trifluoromethyl group and a nitro substituent positioned ortho to the bromine, creating a highly electron-deficient pyridine core. This combination enables selective cross-coupling reactions under mild conditions, with enhanced stability compared to analogous halogenated heterocycles. The molecule’s robust reactivity profile supports efficient integration into complex synthetic architectures.
2-Bromo-5-nitro-3-(trifluoromethyl)pyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromide and electron-deficient pyridine core. The trifluoromethyl and nitro groups provide strong electron-withdrawing effects, enhancing regioselectivity in C–H functionalization and facilitating the construction of complex heterocyclic scaffolds. Its bench stability and compatibility with standard purification methods make it well-suited for multi-step synthesis workflows.
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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-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: