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Structure of 3040304-84-2
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This piperidine-2,6-dione scaffold features a 6-bromobenzo[d]isoxazolyl substituent at the 3-position, delivering enhanced electron-withdrawing character and structural rigidity. The bromine moiety enables downstream cross-coupling transformations, while the diketone core supports metal coordination and hydrogen bonding. This compound serves as a key building block in medicinal chemistry for targeted heterocycle synthesis under standard conditions.
3-(6-Bromobenzo[d]isoxazol-3-yl)piperidine-2,6-dione serves as a versatile building block for the synthesis of bioactive heterocycles, enabling direct coupling reactions via the bromine handle. Its piperidinedione core offers enhanced solubility and stability under standard reaction conditions, facilitating efficient functionalization in medicinal chemistry workflows. The scaffold supports orthogonal transformations and is compatible with palladium-catalyzed cross-coupling protocols, making it ideal for constructing complex molecular architectures in drug discovery.
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Lot numbers can be found on the outside label of a product: