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Structure of 1228079-29-5
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tert-Butyl 1-oxo-1,3-dihydrospiro[indene-2,4'-piperidine]-1'-carboxylate features a spirocyclic architecture integrating an indene core with a piperidine ring, enabling precise stereocontrol in synthesis. The tert-butyl ester group provides stability and ease of deprotection under mild conditions, while the oxo functionality offers a reactive handle for downstream functionalization. This scaffold serves as a key intermediate in constructing complex alkaloid frameworks and bioactive molecules.
tert-Butyl 1-oxo-1,3-dihydrospiro[indene-2,4'-piperidine]-1'-carboxylate serves as a versatile spirocyclic scaffold for medicinal chemistry and natural product synthesis. The indene core provides rigidity and defined stereochemistry, while the piperidine nitrogen and ester functionality enable sequential functionalization. It facilitates efficient access to complex heterocycles via standard transformations such as reductive amination, amide coupling, and cyclization reactions. Bench-stable and amenable to purification by chromatography, it functions effectively in multi-step synthetic sequences requiring structural diversity and stability.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319
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Precautionary Statements : P261-P302+P352
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Lot numbers can be found on the outside label of a product: