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Structure of 27063-93-0
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3-Bromo-2,4-lutidine features a bromine substituent at the 3-position of the lutidine core, delivering a regioselective handle for cross-coupling reactions. The electron-rich aromatic system enhances reactivity in palladium-catalyzed transformations, while the methyl groups provide steric guidance and stability under standard conditions. This compound serves as a key intermediate in the synthesis of functionalized heterocycles.
3-Bromo-2,4-lutidine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its ortho-brominated pyridine framework. The methyl groups at positions 2 and 4 provide steric and electronic modulation, enhancing regioselectivity in C–H functionalization and Suzuki-Miyaura coupling. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for constructing complex heterocyclic scaffolds in API 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-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: