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Structure of 958991-06-5
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Methyl 6-oxopiperidine-3-carboxylate features a cyclic amide scaffold with a ketone at C6 and an ester at C3, enabling direct functionalization at the enolizable α-position. This versatile building block integrates readily into complex heterocycles under mild conditions.
Methyl 6-oxopiperidine-3-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to piperidine-based scaffolds prevalent in medicinal chemistry. Its α,β-unsaturated carbonyl system facilitates Michael additions and cyclizations, while the ester group permits selective reduction or derivatization. The compound exhibits good bench stability and is compatible with a range of standard reaction conditions, making it ideal for constructing heterocyclic cores and functionalized intermediates in API 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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: