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Structure of 148763-41-1
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Methyl N-Boc-piperidine-3-carboxylate is a bench-stable, moisture-tolerant building block featuring a protected piperidine core and ester functionality. This versatile intermediate integrates readily into synthetic sequences requiring nitrogen-directed cyclizations or selective functionalization at the 3-position. The Boc group enables straightforward deprotection under mild acidic conditions, while the methyl ester supports diverse transformations including reduction, hydrolysis, or coupling reactions.
Methyl N-Boc-piperidine-3-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds. The Boc-protected amine and ester functionalities offer orthogonal reactivity, facilitating selective transformations during multistep synthesis. Its bench-stable nature and compatibility with standard coupling and reduction protocols make it well-suited for iterative functionalization and heterocycle construction 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 : 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: