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Structure of 1188265-31-7
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tert-Butyl 3-methoxy-4-oxopiperidine-1-carboxylate features a masked piperidinone scaffold with orthogonal protection, enabling selective functionalization at the nitrogen and carbonyl sites. The methoxy group enhances solubility and modulates reactivity, while the tert-butyl ester provides stability under basic conditions and facilitates clean deprotection. This intermediate supports efficient access to complex nitrogen-containing architectures in medicinal chemistry and natural product synthesis.
tert-Butyl 3-methoxy-4-oxopiperidine-1-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to piperidine-based scaffolds. The protected amine and ketone functionalities offer orthogonal reactivity for selective transformations, while the tert-butoxycarbonyl (Boc) group provides bench stability and ease of removal under mild acidic conditions. Its methoxy substituent enhances solubility and modulates electronic effects, facilitating downstream functionalization in medicinal chemistry and process development workflows.
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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: