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Structure of 4985-92-6
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5-Methylpicolinaldehyde delivers a sterically accessible aldehyde functionality within a nitrogen-containing heterocyclic framework, enabling direct coupling in transition-metal-catalyzed cross-couplings and condensation reactions. This bench-stable reagent integrates readily into synthetic sequences requiring selective C–H functionalization or imine formation under mild conditions.
5-Methylpicolinaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of heterocyclic scaffolds and functionalized aromatic systems. Its aldehyde functionality exhibits reliable reactivity in condensation reactions, including imine formation and Mannich-type cyclizations, while the methyl group provides mild electronic modulation. The compound demonstrates excellent bench stability and compatibility with common protecting group strategies, facilitating straightforward purification and integration into multi-step syntheses.
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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: