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Structure of 1204-86-0
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4-Morpholin-4-yl-benzaldehyde features a morpholine ring appended to the para position of a benzaldehyde scaffold, delivering enhanced solubility and electron-rich character. This combination enables efficient coupling in Suzuki-Miyaura and Ullmann-type transformations. The aldehyde group provides a direct handle for reductive amination or oxime formation, streamlining access to bioactive heterocycles and pharmaceutical intermediates under standard conditions.
4-Morpholin-4-yl-benzaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient construction of biologically active scaffolds. Its aldehyde functionality facilitates nucleophilic addition, reductive amination, and imine formation under standard conditions. The morpholinyl group enhances solubility and modulates electronic properties, while the aromatic core supports further functionalization via electrophilic substitution or cross-coupling reactions. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses of targeted compounds.
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Lot numbers can be found on the outside label of a product: