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Structure of 169206-65-9
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tert-Butyl 4-(2-methoxy-2-oxoethylidene)piperidine-1-carboxylate features a reactive enol ether moiety flanked by a piperidine scaffold, enabling direct integration into cascade cyclizations. This bench-stable, moisture-tolerant building block facilitates rapid access to complex heterocyclic architectures under mild conditions.
tert-Butyl 4-(2-methoxy-2-oxoethylidene)piperidine-1-carboxylate serves as a versatile building block for heterocyclic synthesis, enabling efficient access to piperidine derivatives via Michael addition or reductive amination. The enone functionality facilitates conjugate addition with nucleophiles, while the tert-butoxycarbonyl (Boc) group offers robust protection and ease of removal under mild acidic conditions. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for iterative synthetic strategies in medicinal chemistry and process development.
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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
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: