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Structure of 16727-47-2
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2,6-Bis(benzyloxy)-3-bromopyridine features a pyridine core functionalized with two benzyloxy groups at the 2 and 6 positions and a bromine atom at the 3 position. This configuration enables selective coupling reactions in late-stage diversification of heterocyclic scaffolds. The benzyl ethers provide stability and solubility, while the electrophilic bromine facilitates cross-coupling transformations under mild conditions.
2,6-Bis(benzyloxy)-3-bromopyridine serves as a versatile building block for the synthesis of substituted pyridine scaffolds in medicinal chemistry and materials science. The benzyloxy groups provide orthogonal protection for phenolic functionalities, while the bromine at C3 enables palladium-catalyzed cross-coupling reactions. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient downstream transformations in complex molecule assembly.
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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 : P233-P260-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P340-P362-P403-P405-P501
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Lot numbers can be found on the outside label of a product: