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Structure of 1690-74-0
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Methyl 1-methylpiperidine-2-carboxylate is a sterically hindered, bench-stable piperidine derivative featuring a methyl ester group at the C2 position. This configuration enhances solubility in common organic solvents and facilitates straightforward functionalization in synthetic transformations. The molecule serves as a key intermediate in the construction of bioactive alkaloids and pharmaceutical scaffolds due to its compatibility with diverse coupling and reduction protocols.
Methyl 1-methylpiperidine-2-carboxylate serves as a versatile chiral building block in synthetic organic chemistry, enabling efficient access to piperidine-containing scaffolds. Its methyl ester functionality facilitates subsequent derivatization, while the N-methylpiperidine core provides favorable solubility and stability. The compound exhibits excellent functional group tolerance and is compatible with standard coupling, reduction, and alkylation protocols, making it a practical choice for 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: