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Structure of 2208-59-5
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2-Pyridin-4-yl-1H-benzimidazole integrates a pyridyl heterocycle with a benzimidazole core, delivering enhanced electron delocalization and coordination versatility. This rigid, planar scaffold exhibits strong π-stacking propensity and stable chelation potential, making it ideal for metal-ligand frameworks, catalytic systems, and functional materials in organic electronics and medicinal chemistry applications.
2-Pyridin-4-yl-1H-benzimidazole serves as a versatile heterocyclic building block in medicinal chemistry, enabling the construction of biologically active scaffolds through palladium-catalyzed cross-coupling reactions. Its structural rigidity and dual nitrogen donor sites enhance metal coordination for catalyst design, while its bench stability and ease of purification support scalable synthesis. Functions effectively in C–H functionalization and as a ligand in transition metal catalysis.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: