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Structure of 3274-56-4
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2,4-Diphenyl-1H-pyrrole features a conjugated pyrrole core flanked by two phenyl groups, delivering enhanced electronic delocalization and stability. This electron-rich scaffold integrates readily into π-conjugated systems, serving as a robust building block for functional materials in organic electronics and synthetic intermediates.
2,4-Diphenyl-1H-pyrrole serves as a versatile scaffold for constructing biologically relevant heterocycles and functionalized aromatic systems. Its stability under standard reaction conditions enables straightforward functionalization at the pyrrole ring, facilitating C–H activation and transition-metal-catalyzed coupling reactions. The molecule functions effectively as a building block in synthetic pathways targeting pharmaceutical intermediates and advanced materials.
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Lot numbers can be found on the outside label of a product: