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Structure of 881674-56-2
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This pyrrole aldehyde features a 2-fluorophenyl substituent that enhances electronic modulation and improves solubility in organic solvents. The aldehyde group enables direct coupling in Suzuki-Miyaura and Ullmann-type reactions, while the electron-deficient pyrrole ring facilitates conjugation. Bench-stable under standard conditions, it serves as a key intermediate in synthesizing bioactive heterocycles and functional materials.
5-(2-Fluorophenyl)-1H-pyrrole-3-carbaldehyde serves as a versatile building block for bioactive heterocycles, enabling direct incorporation of fluorinated aryl and aldehyde functionalities in late-stage diversification. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient synthesis of pharmaceutical scaffolds, particularly in kinase inhibitor and CNS-targeted compound development.
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Lot numbers can be found on the outside label of a product: