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Structure of 33042-66-9
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Spiro[indene-1,4'-piperidine] features a rigid spirocyclic architecture that integrates an indene core with a piperidine ring, delivering enhanced conformational stability and defined spatial orientation. This structural motif enables precise molecular positioning in synthetic scaffolds, particularly useful in medicinal chemistry applications requiring controlled three-dimensional presentation. The compound exhibits favorable solubility in common organic solvents and maintains stability under standard bench conditions.
Spiro[indene-1,4'-piperidine] serves as a rigid, three-dimensional scaffold enabling the construction of diverse heterocyclic architectures. Its spirocyclic framework imparts conformational stability and enhances metabolic resistance, making it valuable in medicinal chemistry lead optimization. The piperidine nitrogen facilitates salt formation and modulates basicity, while the indene moiety offers opportunities for functionalization via electrophilic or transition-metal-catalyzed reactions. This compound functions as a versatile building block in the synthesis of bioactive molecules, particularly those requiring defined spatial orientation and enhanced lipophilicity.
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Lot numbers can be found on the outside label of a product: