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Structure of 1060815-64-6
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3-Bromo-6-chloropicolinaldehyde features a sterically accessible pyridine core bearing complementary halogen substituents, enabling selective cross-coupling and functionalization. This bench-stable aldehyde integrates readily into complex molecular architectures under standard conditions.
3-Bromo-6-chloropicolinaldehyde serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds. Its dual halogen substituents provide orthogonal reactivity for Pd-catalyzed cross-coupling reactions, while the aldehyde functionality facilitates imine formation, reductive amination, or cyclization protocols. Bench-stable and compatible with standard purification methods, it functions reliably in multi-step syntheses requiring functional group tolerance and predictable regiochemistry.
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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: